LLC POLPHARMA UA TRADE DATA ANALYSIS
Access comprehensive trade data for Llc Polpharma Ua with ease. Explore trade shipments, top suppliers & buyers, and values without the hassle.
Llc Polpharma Ua – Overview
Eximpedia analyzes Llc Polpharma Ua export and import records, including data from 0 buyers and 5 suppliers. We provide an intelligence report of Llc Polpharma Ua that covers trade statistics, shipment values, quantities, exporters & importers and trade destinations
Llc Polpharma Ua Buyers, Suppliers & Shipments
Llc Polpharma Ua import markets
Explore the Llc Polpharma Ua import market with monthly import values, major importers, HS Codes, key ports, top suppliers, and competitors
TOP IMPORT HS CODE
| HS CODE | USD VALUE | SHIPMENTS | % |
|---|---|---|---|
| 3004900000 | 8.17 | 41 | 27.52 |
| MEDICAMENTS (EXCLUDING GOODS OF HEADING 3002, 3005 OR 3006) CONSISTING OF MIXED OR UNMIXED PRODUCTS FOR THERAPEUTIC OR PROPHYLACTIC USES, PUT UP IN MEASURED DOSES (IINCLUDING THOSE IN THE FORM OF TRANSDERMAL ADMINISTRATION SYSTEMS) OR IN FORMS OR PACKINGS | |||
| 3004500000 | 2.40 | 15 | 10.07 |
| MEDICAMENTS (EXCLUDING GOODS OF HEADING 3002, 3005 OR 3006) CONSISTING OF MIXED OR UNMIXED PRODUCTS FOR THERAPEUTIC OR PROPHYLACTIC USES, PUT UP IN MEASURED DOSES (IINCLUDING THOSE IN THE FORM OF TRANSDERMAL ADMINISTRATION SYSTEMS) OR IN FORMS OR PACKINGS | |||
| 3307900000 | 1.51 | 11 | 7.38 |
| PRE-SHAVE, SHAVING OR AFTER-SHAVE PREPARATIONS, PERSONAL DEODORANTS, BATH PREPARATIONS, DEPILATORIES AND OTHER PERFUMERY, COSMETIC OR TOILET PREPARATIONS, NOT ELSEWHERE SPECIFIED OR INCLUDED, PREPARED ROOM DEODORISERS, WHETHER OR NOT PERFUMED OR HAVING DI | |||
| 2106909200 | 1.46 | 45 | 30.20 |
| FOOD PREPARATIONS NOT ELSEWHERE SPECIFIED OR INCLUDED | |||
| 3004200000 | 1.27 | 5 | 3.36 |
| MEDICAMENTS (EXCLUDING GOODS OF HEADING 3002, 3005 OR 3006) CONSISTING OF MIXED OR UNMIXED PRODUCTS FOR THERAPEUTIC OR PROPHYLACTIC USES, PUT UP IN MEASURED DOSES (IINCLUDING THOSE IN THE FORM OF TRANSDERMAL ADMINISTRATION SYSTEMS) OR IN FORMS OR PACKINGS | |||
TOP IMPORT COUNTRY
| COUNTRY | USD VALUE | SHIPMENTS | % |
|---|---|---|---|
| POLAND | 13.92 | 79 | 53.02 |
| EUROPEAN UNION | 2.88 | 58 | 38.93 |
| ITALY | 0.27 | 2 | 1.34 |
| FRANCE | 0.22 | 4 | 2.68 |
| GREECE | 0.12 | 5 | 3.36 |
TOP IMPORT PORTS
| PORT NAME | USD VALUE | SHIPMENTS | % |
|---|---|---|---|
| UA100380 | 17.41 | 146 | 97.99 |
| UA100290 | 0.00 | 3 | 2.01 |
TOP IMPORT COMPETITORS
| COMPANY | USD VALUE | SHIPMENTS |
|---|---|---|
| MINISTRY OF HEALTH | 206.51 | 8344 |
| SOCIAL SECURITY INSTITUTION | 231.08 | 35 |
| BADM LIMITED LIABILITY COMPANY | 394.73 | 5166 |
| JV OPTIMA FARM LIMITED | 400.43 | 5786 |
| TURKISH PHARMACISTS ASSOCIATION ECONOMIC ENTERPRISE | 536.15 | 2196 |
TOP IMPORT SUPPLIERS
| COMPANY | USD VALUE | SHIPMENTS |
|---|---|---|
| TANNER PHARMA CH GMBH ON BEHALF OF MAXAID | 117.29 | 15 |
| BIOGEN INTERNATIONAL GMBH | 127.48 | 115 |
| BOEHRINGER INGELHEIM | 146.49 | 839 |
| BMED INTERNATIONAL BUSINESS COMPANY LIMITED | 150.27 | 163 |
| GEN ILAÇ INTERNATIONAL TRADING LIMITED | 244.44 | 236 |
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Llc Polpharma Ua Import Shipments
Discover the Llc Polpharma Ua with product description, import values, quantities, exporter name, country of origin and key destinations.
| HSN Code | Product Description | Imports | Exporter | Origin | Destination | Qty. |
|---|---|---|---|---|---|---|
| 1704905500 | 1. SORE THROAT LASTILLES, PACKAGED FOR RETAIL TRADE, DOES NOT CONTAIN COMPONENTS OF ANIMAL ORIGIN IN THE ORIGINAL PACKAGING, NOT IN AEROSOL PACKAGING: HERBALOR FOR THROAT, 3.5G LASTILLES, 8 LASTILLES IN A BLISTER; PER 2 BLISTERS IN A CARDBOARD BOX NO. 16 SERIES: 140723 - 26600 EXP. EXPIRY DATE - 01.07.2025 TRADEMARK - HERBALOR. MANUFACTURER: VTO """"EVA"""" S.A., POLAND, FOR PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A. , POLAND. COUNTRY OF MANUFACTURE - POLAND (PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION |  |
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EUROPEAN UNION | UKRAINE | 0 |
| 2106909200 | 1. DIETARY SUPPLEMENT WITHOUT MILK FATS, SUCROSE, ISOGLUCOSE, GLUCOSE, STARCH, IN PRIMARY PACKAGING, NOT IN AEROSOL PACKAGING: OLIDETRIM 4000, SOFT GELATIN CAPSULES, 15 CAPSULES IN BLISTERS; 4 BLISTERS IN CARDBOARD BOX NO. 60 SERIES: 030523 - 21600 EXP EXPIRY DATE - 01.05.2025 TRADEMARK - OLIDETRIM. MANUFACTURER: PHARMACEUTICAL PLANT ""POLPHARMA"" S.A., BRANCH ""MEDANA"" WM. SIERADZ, POLAND """"OLIDETRIM"""", M WHICH TWIST-OFF TYPE GELATIN CAPSULES #30 (15 X2): 15 CAPSULES IN A BLISTER; 2 BLISTERS IN A CARDBOARD BOX. SERIES: 010823 -12000 UP. EXPIRY DATE - 01.08.2025 TRADEMARK - OLIDETRIM. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A., DEPARTMENT """"MEDANA"""" VM. SIERADZ, POLAND COUNTRY OF PRODUCTION - POLAND (PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
|
EUROPEAN UNION | UKRAINE | 0 |
| 2106909200 | 1. DIETARY SUPPLEMENT WITHOUT MILK FAT, SUCROSE, ISOGLUCOSE, GLUCOSE, STARCH, IN PRIMARY PACKAGING, NOT IN AEROSOL PACKAGING: SUPEROPTIC, CAPSULES 850 MG, 10 CAPSULES IN A BLISTER; LISTER IN A CARDBOARD BOX NO. 30. SERIES: 020723 - 2560 EXPIRY DATE - 07/01/2025 TRADEMARK - SUPEROPTIC. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A., DEPARTMENT """"MEDANA"""" VM. SIERADZ, POLAND COUNTRY OF PRODUCTION - POLAND (PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
|
EUROPEAN UNION | UKRAINE | 0 |
| 3004900000 | 1. DRUGS (DRUGS FOR HUMANS) PACKAGED FOR RETAIL TRADE IN AEROSOL PACKAGING: ALLERTEK(R), COATED TABLETS, 10MG OF 20 TABLETS IN A BLISTER, 1 BLISTER IN A CARDBOARD BOX. ACTIVE INGREDIENT : 1 TABLET, COVERED WITH A SHELL, CONTAINS CETYRIZINE HYDROCHLORIDE 10MG. SERIES: 010623 - 15090 EXP. EXPIRY DATE - 01.06.2027 UA/6422/02/01 19.05.17 - UNLIMITED. TRADEMARK: ALLERTEK. MANUFACTURER: PHARMACEUTICAL PLANT """"POLFAR"" MA"""" S.A., POLAND . ALLERTEK(R), COATED TABLETS, 10MG, 7 TABLETS IN A BLISTER, 1 BLISTER IN A CARDBOARD BOX. ACTIVE INGREDIENT: 1 COATED TABLET CONTAINS CETIRIZINE HYDROCHLORIDE 10MG. SERIES: 010923 - 9920 UP. EXPIRY DATE - 01.09.2027UA/6422/02/01 19.05.17 - UNLIMITED. TRADEMARK: ALLERTEK. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A., POLAND. INDAPEN SR, MODIFIED RELEASE COATED TABLETS 1.5 MG 15 TABLETS BLISTER; 2 BLISTERS IN CARDBOARD BOX NO. 30. ACTIVE INGREDIENT: 1 TABLET CONTAINS INDAPAMIDA 1.5MG. SERIES: 50823 - 14778UP. EXPIRY DATE - 01.08.2025UA/0877/02/01 19.10.2016 - UNLIMITED. TRADEMARK: INDAPEN. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A., POLAND. PHYTOLYSIN(R), PASTE FOR PREPARATION OF SUSPENSION FOR ORAL USE, 100 G IN A TUBE; 1 TUBE IN A CARTON BOX. ACTIVE INGREDIENT: 100 G PASTE CONTAINS EXTRACT OF CONCENTRATED MIXTURE OF MEDICINAL PLANT RAW MATERIALS [AGROPYRON REPENS (L.)BEAUV., RHIZOMA) 12.5 G, ONION PEEL (ALLIUM CEPA L., SQUAMA) 5 G, LEAF BIRCH (BETULA P ENDULA ROTH; BETULA PUBESCENS EHRH., FOLIUM) 10 G, FENUGREEN SEEDS (TRIGONELLA FOENUM GRAECUM L., SEMEN) 15 G, PARSLEY ROOTS (PETROSELINUM SATIVUM HOFFM., RADIX) 17.5 G, SOLIDAGOVIRGAUREA L., HERBA) 5 G, EQUISETUM ARVENSE L., HERBA HERBS 10 G, LUVORIS ROOT (LEVISTICUM OFFICINALE KOCH, RADIX) 10 G, BITTER CABBAGE HERBS (POLYGONUM AVICULARE L., HERBA) 15 G] (1:1.3 1.6) (EXTRACTING ETHANOL 45 %) 67.2 G. SERIES: 630823 - 10450 PACK. EXPIRY DATE - 01.07.2026UA/0471/01/01 22.10.18 - UNLIMITED. TRADEMARK - PHYTOLYZIN. MANUFACTURER: TOV HERBAPOL WARSAW, POLAND. ESPIRO, FILM-COATED TABLETS, 50 MG, 10 TABLETS IN A BLISTER, 3 BLISTERS IN A CARDBOARD BOX #30. ACTIVE INGREDIENT: 1 FILM-COATED TABLET CONTAINS 50 MGEPLERENONE. SERIES: 40323 - 3780 UP. EXPIRY DATE - 01.03.2027UA/18267/01/02 25.08.20 - 25.08.25 TRADEMARK: ESPIRO. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A., POLAND. COUNTRY OF PRODUCTION - POLAND (PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
|
POLAND | UKRAINE | 0 |
| 3307900000 | 1. MEDICAL PRODUCT: SUPEROPTIK(TM) AQUA, EYE DROPS 5ML IN VIALS #2. SERIES: 05VP1023 - 27844 EXP. EXPIRY DATE - 10.01.2025 TRADEMARK - SUPEROPTIK. MANUFACTURER: WARSAW PHARMACEUTICAL PLANT """" POLFA"""" JSC, POLAND/WARSZAWSKIE ZAKLADY FARMACEUTYCZNE POLFASPOLKA AKCYJNA, POLAND. SUPEROPTIK(TM) AQUA, EYE DROPS OF 5ML IN VIALS #2. SERIES: 06VP1023 - 27495 EXPIRY DATE - 01.10.2025 TRADEMARK - SUPEROPTIC. MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT """"POLFA"" JSC, POLAND/ WARSZAWSKIEZAKLADY FARMACEUTYCZNE POLFA SPOLKA AKCYJNA, POLAND. SUPEROPTIC(TM) AQUA, 5ML EYE DROPS IN VIALS #2. SERIES: 07VP1023 - 27950 UP. EXPIRY DATE - 01.10.2025 TRADEMARK - SUPEROPTIC. MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT """"POLFA"""" JSC, POLAND/ WARSZAWSKIEZAKLADY FARMACEUTYCZNE POLFA SPOLKA AKCYJNA, POLAND. SUPEROPTIC(TM) AQUA, 5ML EYE DROPS IN VIALS #2. SERIES: 10VP1023 - 27947 UP. EXPIRY DATE - 01.10.2025 TRADEMARK - SUPEROPTIC. MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT """"POLFA"""" JSC, POLAND/ WARSZAWSKIEZAKLADY FARMACEUTYCZNE POLFA SPOLKA AKCYJNA, POLAND. SUPEROPTIC(TM) AQUA, 5ML EYE DROPS IN VIALS #2. SERIES: 12VP1023 - 27800 PU. EXPIRY DATE - 01.10.2025 TRADEMARK - SUPEROPTIC. MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT """"POLFA"""" JSC, POLAND/ WARSZAWSKIEZAKLADY FARMACEUTYCZNE POLFA SPOLKA AKCYJNA, POLAND. SUPEROPTIC(TM) AQUA, 5ML EYE DROPS IN VIALS #2. SERIES: 11VP1023 - 28050 UP. EXPIRY DATE - 01.10.2025 TRADEMARK - SUPEROPTIC. MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT """"POLFA"""" JSC, POLAND/ WARSZAWSKIEZAKLADY FARMACEUTYCZNE POLFA SPOLKA AKCYJNA, POLAND. SUPEROPTIC(TM) COMPLETE, 10ML EYE DROPS IN VIAL #1. SERIES: 03ZH0323 - 22400 UP. EXPIRY DATE - 01.03.2025 TRADEMARK - SUPEROPTIC MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT """"POLFA"""" JSC, POLAND/ WARSZAWSKIEZAKLADY FARMACEUTYCZNE POLFA SPOLKA AKCYJNA, POLAND. SUPEROPTIC(TM) COMPLETE, 10ML EYE DROPS IN VIAL #1. SERIES: 01ZH0923 - 22400 UP. EXPIRY DATE - 01.09.2025 TRADEMARK - SUPEROPTIC MANUFACTURER: WARSAWSKY PHARMACEUTICAL PLANT """"POLFA"""" JSC, POLAND/ WARSZAWSKIEZAKLADY FARMACEUTYCZNE POLFA SPOLKA AKCYJNA, POLAND. SUPEROPTIC(TM) COMPLETE, 10ML EYE DROPS IN VIAL #1. SERIES: 02ZH0923 - 22400 UP. EXPIRY DATE - 01.09.2025 TRADEMARK - SUPER OPTICS MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT """"POLFA"""" JSC, POLAND/ WARSZAWSKIEZAKLADY FARMACEUTYCZNE POLFA SPOLKA AKCYJNA, POLAND. COUNTRY OF PRODUCTION - POLAND (PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
|
EUROPEAN UNION | UKRAINE | 0 |
| 3004200000 | 1. MEDICINES (DRUGS FOR HUMANS CONTAINING ANTIBIOTICS) PACKAGED FOR RETAIL TRADE NOT IN AEROSOL PACKAGING: TOBROSOPT(R)-DEX, EYE DROPS, SUSPENSION (3.0 MG/1.0 MG) IN 1 ML; 5 ML IN A VIAL- DROPPERS; PER 1 VIAL - DROPPERS IN CARDBOARD BOX NO. 1. ACTIVE INGREDIENT: 1 ML OF SUSPENSION CONTAINS TOBRAMYCIN 3 MG AND DEXAMETHASONE 1 MG. SERIES: 01ZB0623 - 12264 UP. EXPIRY DATE - 01.06.2025 RP UA/14326/01/01 06.04.20 - UNLIMITED TRADEMARK - TOBROSOPT(R)-DEX. MANUFACTURER: WARSAW POLFA PHARMACEUTICAL PLANT JSC, POLAND COUNTRY OF PRODUCTION - POLAND(PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
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POLAND | UKRAINE | 0 |
| 3004320000 | 1. MEDICINES (DRUGS FOR HUMANS CONTAINING CORTICOSTEROID HORMONES), PACKAGED FOR RETAIL SALE, NOT IN AEROSOL PACKAGING: DEXAMETHASONE VFZ EYE DROPS, SUSPENSION, 1 MG/ML OF 5 ML IN A CONTROLLED DROPPER VIAL FIRST DISCLOSURE; PER 1 VIAL - SPOTS WITH CONTROLLED FIRST OPENING IN A CARTON PACKAGE ACTIVE SUBSTANCE: 1 ML OF SUSPENSION CONTAINS 1 MG OF DEXAMETHASONE. SERIES: 01UH0223 - 46368 UP. EXPIRY DATE - 01.02.2025UA/2543/01/01 09.04.20 - UNLIMITED. TRADEMARK - DEXAMETHASONE MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT POLFA JSC, POLAND. COUNTRY OF MANUFACTURE - POLAND (PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
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POLAND | UKRAINE | 0 |
| 3004390000 | 1. MEDICINES (MEDICINES FOR HUMANS CONTAINING OTHER HORMONES) PACKAGED FOR RETAIL TRADE, NOT IN AEROSOL PACKAGING: BIMICAN(R) ECO, EYE DROPS, SOLUTION 0.3 MG/ML, 3 ML PREPARATION VIAL-DROPPER, PO 1 VIAL IN A CARDBOARD BOX. ACTIVE INGREDIENT: 1 ML OF SOLUTION CONTAINS 0.3 MG OF BIMAPROST. SERIES: 01ZA1023 - 25568 PACK. EXPIRY DATE - 01.10.2025 UA/16893/01/0111.04.2023 - UNLIMITED. TRADE BRAND: BIMICAN ECO. MANUFACTURER: WARSAWSKY PHARMACEUTICAL PLANT POLFA JSC, POLAND BIMICAN(R) ECO, DROPPERS, SOLUTION 0.3 MG/ML, PO 3 ML OF THE MEDICATION IN A DROPPER VIAL, 1 VIAL IN A CARDBOARD BOX. ACTIVE INGREDIENT: 1 ML OF SOLUTION CONTAINS 0.3 MG OF BIMAPROST. SERIES: 02ZA0523 - 184 UNITS. EXPIRY DATE - 01.05.2025 UA/16893/01/0111.04.2023 - UNLIMITED. TRADEMARK: BIMIKAN ECO. MANUFACTURER: WARSAWSKY PHARMACEUTICAL PLANT POLFA JSC, POLAND COUNTRY OF PRODUCTION - POLAND (PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
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POLAND | UKRAINE | 0 |
| 3004900000 | 1. MEDICINES (DRUGS FOR HUMANS) PACKAGED FOR RETAIL TRADE IN AEROSOL PACKAGING: DORZOPTIK COMBI ECO, EYE DROPS, SOLUTION 20 MG/ML+5 MG/ML, 5 ML OF THE DRUG IN A DROPPER VIAL, 1 VIAL IN A CARD HIS BOXES №1. ACTIVE INGREDIENT: 1 ML EYE DROPS, SOLUTION, CONTAINS 20 MG DORZOLAMIDE (IN THE FORM OF 22.26 MG DORZOLAMIDE HYDROCHLORIDE) AND 5 MG TIMOLOL (IN THE FORM OF 6.83 MG TIMOLOL MALEATE). SERIES: 02ZF0923 - 15630 PACK. EXPIRY DATE - 01.09.2025 UA/18413/01/0130.10.20 - 30.10.25 TRADEMARK: DORZOPTIK KOMBI ECO. MANUFACTURER: WARSAWSKY PHARMACEUTICAL PLANT POLFA JSC, POLAND. DORZOPTIK COMBIEKO, EYE DROPS, SOLUTION 20 MG/ML+5 MG/ML, 5 ML OF THE DRUG VIAL-DROPPER, 1 VIAL IN CARDBOARD BOX #1. ACTIVE INGREDIENT: 1 ML EYE DROP, SOLUTION, CONTAINS 20 MG DORZOLAMIDE (AS 22.26 MG DORZOLAMIDE HYDROCHLORIDE) AND 5 MG TIMOLOL (AS 6.83 MG TIMOLOL MALEATE). SERIES: 04ZF1123 - 15648 PACK. EXPIRY DATE - 01.11.2025 UA/18413/01/0130.10.20 - 30.10.25 TRADEMARK: DORZOPTIK COMBI ECO. MANUFACTURER: WARSAWSKY PHARMACEUTICAL PLANT POLFA JSC, POLAND. DORZOPTIK COMBIEKO, EYE DROPS, SOLUTION 20 MG/ML+5 MG/ML, 5 ML OF THE DRUG VIAL-DROPPER, 1 VIAL IN CARDBOARD BOX #1. ACTIVE INGREDIENT: 1 ML EYE DROP, SOLUTION, CONTAINS 20 MG DORZOLAMIDE (AS 22.26 MG DORZOLAMIDE HYDROCHLORIDE) AND 5 MG TIMOLOL (AS 6.83 MG TIMOLOL MALEATE). SERIES: 05ZF1123 - 15008 PACK. EXPIRY DATE - 01.11.2025 UA/18413/01/0130.10.20 - 30.10.25 TRADEMARK: DORZOPTIK COMBI ECO. MANUFACTURER: WARSAWSKY PHARMACEUTICAL PLANT POLFA JSC, POLAND. DORZOPTIK COMBIEKO, EYE DROPS, SOLUTION 20 MG/ML+5 MG/ML, 5 ML OF THE DRUG VIAL-DROPPER, 1 VIAL IN CARDBOARD BOX #1. ACTIVE INGREDIENT: 1 ML EYE DROP, SOLUTION, CONTAINS 20 MG DORZOLAMIDE (AS 22.26 MG DORZOLAMIDE HYDROCHLORIDE) AND 5 MG TIMOLOL (AS 6.83 MG TIMOLOL MALEATE). SERIES: 06ZF1123 - 15086 PACK. EXPIRY DATE - 01.11.2025 UA/18413/01/0130.10.20 - 30.10.25 TRADEMARK: DORZOPTIK COMBI ECO. MANUFACTURER: WARSAWSKY PHARMACEUTICAL PLANT POLFA JSC, POLAND. DORZOPTIK COMBIEKO, EYE DROPS, SOLUTION 20 MG/ML+5 MG/ML, 5 ML OF THE DRUG VIAL-DROPPER, 1 VIAL IN CARDBOARD BOX #1. ACTIVE INGREDIENT: 1 ML EYE DROP, SOLUTION, CONTAINS 20 MG DORZOLAMIDE (AS 22.26 MG DORZOLAMIDE HYDROCHLORIDE) AND 5 MG TIMOLOL (AS 6.83 MG TIMOLOL MALEATE). SERIES: 07ZF1123 - 14976 PACK. EXPIRY DATE - 01.11.2025 UA/18413/01/0130.10.20 - 30.10.25 TRADEMARK: DORZOPTIK COMBI ECO. MANUFACTURER: WARSAWSKY PHARMACEUTICAL PLANT POLFA JSC, POLAND. DORZOPTIK COMBIEKO, EYE DROPS, SOLUTION 20 MG/ML+5 MG/ML, 5 ML OF THE DRUG VIAL-DROPPER, 1 VIAL IN CARDBOARD BOX #1. ACTIVE INGREDIENT: 1 ML EYE DROP, SOLUTION, CONTAINS 20 MG DORZOLAMIDE (AS 22.26 MG DORZOLAMIDE HYDROCHLORIDE) AND 5 MG TIMOLOL (AS 6.83 MG TIMOLOL MALEATE). SERIES: 02ZF0823 - 15566 PACK. EXPIRY DATE - 01.08.2025 UA/18413/01/0130.10.20 - 30.10.25 TRADEMARK: DORZOPTIK COMBI ECO. MANUFACTURER: WARSAWSKY PHARMACEUTICAL PLANT POLFA JSC, POLAND. COUNTRY OF PRODUCTION - POLAND (PL ). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
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POLAND | UKRAINE | 0 |
| 3307900000 | 1. MEDICAL PRODUCT: SUPEROPTIK(TM) AQUA, EYE DROPS 5ML IN VIALS #2. SERIES: 02VP0623 - 27835 EXP. EXPIRY DATE - 01.06.2025 TRADEMARK - SUPEROPTIK. MANUFACTURER: WARSAW PHARMACEUTICAL PLANT """" POLFA"""" JSC, POLAND/WARSZAWSKIE ZAKLADY FARMACEUTYCZNE POLFASPOLKA AKCYJNA, POLAND. SUPEROPTIK(TM) AQUA, EYE DROPS OF 5ML IN VIALS #2. SERIES: 03VP0723 - 14400 EXP. EXPIRY DATE - 01.07.2025 TRADEMARK - SUPEROPTIC. MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT """"POLFA"" JSC, POLAND/ WARSZAWSKIEZAKLADY FARMACEUTYCZNE POLFA SPOLKA AKCYJNA, POLAND. SUPEROPTIC(TM) AQUA, 5ML EYE DROPS IN VIALS #2. SERIES: 03VP0623 - 27800 UP. EXPIRY DATE - 01.06.2025 TRADEMARK - SUPEROPTIC. MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT """"POLFA"""" JSC, POLAND/ WARSZAWSKIEZAKLADY FARMACEUTYCZNE POLFA SPOLKA AKCYJNA, POLAND. COUNTRY OF PRODUCTION - POLAND (PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
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EUROPEAN UNION | UKRAINE | 0 |
| 3004200000 | 1. MEDICINES (DRUGS FOR HUMANS CONTAINING ANTIBIOTICS) PACKAGED FOR RETAIL TRADE NOT IN AEROSOL PACKAGING: TSYPRONEX(R), EYE AND EAR DROPS, 0.3% SOLUTION OF 5 ML IN POLYETHYLENE BOTTLE - DROPPER; 1 VIAL IN CARDBOARD BOX NO. 1. ACTIVE INGREDIENT: 1 ML OF SOLUTION CONTAINS 3 MG OF CIPROFLOXACIN IN THE APPEARANCE OF CIPROFLOXACIN HYDROCHLORIDE MONOHYDRATE 3.5 MG. SERIES: 03VV0923 - 17740 EXP EXPIRY DATE - 09/01/2026 UA/14617/01/01 08/25/20 - UNLIMITED. TRADEMARK: CYPRONEX. MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT POLFA JSC, POLAND CYPRONEX(R), EYE AND EAR DROPS, SOLUTION 0 .3% 5 ML IN A POLYETHYLENE BOTTLE - DROPPER; PO 1 VIAL IN CARDBOARD BOX NO. 1. ACTIVE INGREDIENT: 1 ML OF SOLUTION CONTAINS 3 MG CIPROFLOXACIN AS CIPROFLOXACIN HYDROCHLORIDE MONOHYDRATE 3.5 MG. SERIES: 04VV0923 - 17600UP. EXPIRY DATE - 01.09.2026 UA/14617/01/0125.08.20 - UNLIMITED. TRADE MARK: CIPRONEKS. MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT POLFA JSC, POLAND CYPRONEX(R), DROP AND EAR SOLUTION, 0.3% PO 5 ML V POLYETHYLENE BOTTLE - DROPPER; PO 1 VIAL IN CARDBOARD BOX NO. 1. ACTIVE INGREDIENT: 1 ML OF SOLUTION CONTAINS 3 MG OF CIPROFLOXACIN IN THE FORM OF CIPROFLOXACIN HYDROCHLORIDE MONOHYDRATE 3.5 MG. SERIES: 05VV0923 - 17838UP. EXPIRY DATE - 01.09.2026 UA/14617/01/0125.08.20 - UNLIMITED. TRADE MARK: CIPRONEKS. MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT POLFA JSC, POLAND CYPRONEX(R), DROP AND EAR SOLUTION, 0.3% PO 5 ML V POLYETHYLENE BOTTLE - DROPPER; PO 1 VIAL IN CARDBOARD BOX NO. 1. ACTIVE INGREDIENT: 1 ML OF SOLUTION CONTAINS 3 MG OF CIPROFLOXACIN IN THE FORM OF CIPROFLOXACIN HYDROCHLORIDE MONOHYDRATE 3.5 MG. SERIES: 07VV0923 - 17723UP. EXPIRY DATE - 01.09.2026 UA/14617/01/0125.08.20 - UNLIMITED. TRADE MARK: CIPRONEKS. MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT POLFA JSC, POLAND CYPRONEX(R), DROP AND EAR SOLUTION, 0.3% PO 5 ML V POLYETHYLENE BOTTLE - DROPPER; PO 1 VIAL IN CARDBOARD BOX NO. 1. ACTIVE INGREDIENT: 1 ML OF SOLUTION CONTAINS 3 MG OF CIPROFLOXACIN IN THE FORM OF CIPROFLOXACIN HYDROCHLORIDE MONOHYDRATE 3.5 MG. SERIES: 06VV0923 - 17635UP. EXPIRY DATE - 01.09.2026 UA/14617/01/0125.08.20 - UNLIMITED. TRADEMARK: TSYPRONEKS. MANUFACTURER: WARSAWSKIE PHARMACEUTICAL PLANT POLFA JSC, POLAND COUNTRY OF PRODUCTION - POLAND (PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
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POLAND | UKRAINE | 0 |
| 3004500000 | 1. MEDICAL REMEDIES (MEDICINES FOR HUMANS) CONTAINING VITAMINS PACKAGED FOR RETAIL TRADE NOT IN AEROSOL DUMPING: GAZOLIN (R) COMBI, NASAL SPRAY, SOLUTION, (1.0 MG + 50 MG)/ML, 10 MLU VIAL DROPLETS; 1 VIAL OF SOLUTION IN CARDBOARD BOX NO. 1. ACTIVE INGREDIENT: 1 ML OF SOLUTION CONTAINS: 1 MG OF XYLOMETHAZOLINE HYDROCHLORIDE AND 50 MG OF DEXPANTHENOL; ONE SPRAY OF 0.1 ML OF SOLUTION CONTAINS 0.1 MG OF XYLOMETHAZOLINE HYDROCHLORIDE AND 5 MG OF DEXPANTHENOL. SERIES: 161023 - 45943 EXPIRY DATE - 01.10.2026 UA/16346/01/01 29.09.22 - UNLIMITED. TRADEMARK: GALAZOLIN(R) COMBI. MANUFACTURER: PHARMACEUTICAL PLANT ""POLPHARMA"" S.A. MEDANA DEPARTMENT IN SIERADZ (MANUFACTURING, PRIMARY AND SECONDARY PACKAGING, CONTROL AND BATCH RELEASE), POLAND WARSAW POLFA PHARMACEUTICAL PLANT JSC (BATCH CONTROL AND RELEASE), POLAND GALAZOLIN(R) COMBI, NASAL SPRAY, SOLUTION , (1.0 MG + 50 MG) /ML, PER 10 ML DROPPER VIAL; 1 VIAL WITH SOLUTION IN CARDBOARD BOX NO. 1. ACTIVE SUBSTANCE: 1 ML OF SOLUTION CONTAINS: 1 MG OF XYLOMETHAZOLINE HYDROCHLORIDE AND 50 MG OF DEXPANTHENOL; ONE SPRAY OF 0.1 ML OF SOLUTION CONTAINS 0.1 MG OF XYLOMETHAZOLINE HYDROCHLORIDE AND 5 MG OF DEXPANTHENOL. SERIES: 151023 - 4891 UP. EXPIRY DATE - 01.10.2026 UA/16346/01/01 29.09.22 - UNLIMITED. TRADEMARK: GALAZOLIN(R) COMBI. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A. MEDANA DEPARTMENT IN SIERADZ (MANUFACTURING, PRIMARY AND SECONDARY PACKAGING, CONTROL AND BATCH RELEASE), POLAND WARSAW POLFA PHARMACEUTICAL PLANT JSC (BATCH CONTROL AND RELEASE), POLAND COUNTRY OF PRODUCTION - POLAND(PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
|
POLAND | UKRAINE | 0 |
| 3004900000 | 1. MEDICINES (DRUGS FOR HUMANS) PACKAGED FOR RETAIL TRADE IN AEROSOL PACKAGING: POLAPRIL, SOLID CAPSULES OF 5.0 MG; 14 CAPSULES IN A BLISTER; 2 BLISTERS IN A CARDBOARD BOX NO. 28. ACTIVE INGREDIENT: 1 CAPSULE MI TAKE 5 MG RAMIPRIL SERIES: 21223 - 9452 EXP. EXPIRY DATE - 01.12.2025UA/4441/01/03 26.01.21 - UNLIMITED. TRADEMARK: POLAPRIL. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A., POLAND. ROMAZYK, TABLETS, COVERED WITH A FILM COVER, 10 MG OF 10 TABLETS IN A BLISTER; 3 BLISTERS IN A CARDBOARD BOX NO. 30. ACTIVE INGREDIENT: 1 FILM-COATED TABLET CONTAINS ROSUVASTATIN 10MG, EQUIVALENT TO 10.4MG ROSUVASTATIN CALCIUM. SERIES: 21123 -10800 UP. EXPIRY DATE - 01.11.2025 TRADEMARK: ROMAZYK. UA/13299/01/02 22.10.18 - UNLIMITED MANUFACTURER: ""POLPHARMA"" S.A. PHARMACEUTICAL PLANT, POLAND. PYRANTELPOLPHARMA, ORAL SUSPENSION, 250 MG/5 ML OF 15 ML IN A VIAL, 1 VIAL WITH A DRILL IN A CARDBOARD BOX. ACTIVE INGREDIENT: 5 ML OF SUSPENSION CONTAINS PYRANTEL (AS PYRANTEL PAMOATE) 250 MG. SERIES: 010823 - 19440 UP. EXPIRY DATE - 01.08.2026 UA/9225/01/01 31.10.19 - UNLIMITED. TRADEMARK: PYRANTEL POLPHARMA. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A. MEDANA DEPARTMENT IN SIERADZ, POLAND COUNTRY OF PRODUCTION - POLAND(PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
|
POLAND | UKRAINE | 0 |
| 2106909200 | 1. DIETARY SUPPLEMENT TO THE DIET WITHOUT THE CONTENT OF MILK FAT, SUCROSE, ISOGLUCOSE, GLUCOSE, STARCH, IN THE ORIGINAL PACKAGING, NOT IN AN AEROSOL PACKAGING: ""OLIDETRIM"", SOFT GELATIN CAPSULES OF THE TWIST-OFF TYPE NO. 30 (15 X 2): PER 15 CAPSULES IN A BLISTER; 2 BLISTERS IN A CARDBOARD BOX. SERIES: 010623 - 26014 UNITS. EXPIRY DATE - 01.06.2025. TRADE MARK - OLIDETRIM. MANUFACTURER: PHARMACEUTICAL PLANT ""POLPHARMA"" S.A., BRANCH ""MEDANA"" VM. .SIERADZ, POLAND OLIDETRIM 2000, SOFT GELATIN CAPSULES, BLISTERS OF 15 CAPSULES; 4 BLISTERS IN A CARDBOARD BOX #60. SERIES: 010823 - 41403 PACK. EXPIRY DATE - 01.08.2025. TRADE MARK - OLIDETRIM. MANUFACTURER: ""POLPHARMA"" S.A. PHARMACEUTICAL PLANT, ""MEDANA"" BRANCH, SIERADZ, POLAND. COUNTRY OF MANUFACTURE - POLAND (PL). MARKING IS AVAILABLE AND MEETS THE STANDARDS SET BY THE LEGISLATION.""" | |
|
EUROPEAN UNION | UKRAINE | 0 |
| 2106909200 | 1. DIETARY SUPPLEMENT TO THE DIET WITHOUT THE CONTENT OF PRODUCTS OF ANIMAL ORIGIN, MILK FATS, SUCROSE, ISOGLUCOSE, GLUCOSE, STARCH, IN THE PRIMARY PACKAGING, NOT IN AEROSOL PACKAGING: PHYTOLISIN(R) NEPHROCAPSULE(PHYTOLISIN(R)NEFROCAPS) NO. 30. SERIES: 010623 - 4320 PACK. EXPIRY DATE - 06/01/2026. TRADE MARK - PHYTOLYSIN NEPHROCAPSULES. MANUFACTURER: ""POLPHARMA"" S.A. PHARMACEUTICAL PLANT, POLAND. COUNTRY OF MANUFACTURE - POLAND (PL). MARKING IS AVAILABLE AND MEETS THE STANDARDS SET BY THE LEGISLATION.""" | |
|
EUROPEAN UNION | UKRAINE | 0 |
| 3307900000 | 1. MEDICAL PRODUCT: SUPEROPTIK(TM) COMPLETE, EYE DROPS 10 ML IN BOTTLE NO. 1. SERIES: 02ZH0323 - 15200 UNITS. EXPIRATION DATE - 03.01.2025TRADE MARK - SUPEROPTIKMANUFACTURER: WARSAW PHARMACEUTICAL PLANT ""POLFA"" JSC, POLAND/WARSZAWSKIE ZAKLADY FARMACEUTYCZNE POLFASPOLKA AKCYJNA, POLAND. COUNTRY OF MANUFACTURE - POLAND (PL). MARKING IS AVAILABLE AND MEETS THE STANDARDS SET BY THE LEGISLATION.""" | |
|
POLAND | UKRAINE | 0 |
| 2106909200 | 1. DIETARY SUPPLEMENT WITHOUT DAIRY FAT, SUCROSE, ISOGLUCOSE, STARCH, IN PRIMARY PACKAGING, NOT IN AEROSOL PACKAGING: OLIDETRIM 2000, SOFT GELATIN CAPSULES, 30 CAPSULES BLISTERS; 3 BLISTERS IN CARDBOARD BOX NO. 90 SERIES: 010324 - 12800 EXPIRY DATE - 01.03.2026 TRADEMARK - OLIDETRIM. MANUFACTURER: PHARMACEUTICAL PLANT ""POLPHARMA"" S.A., DEPARTMENT ""MEDANA"" WM. SIERADZ, POLAND COUNTRY OF PRODUCTION - POLAND (PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
|
EUROPEAN UNION | UKRAINE | 0 |
| 2106909890 | 1. PRODUCT IN THE FORM OF AQUEOUS SOLUTION FOR ORAL USE WITH VITAMIN D3 THAT DOES NOT EXCEED THREE RECOMMENDED AVERAGE DAILY INTAKE (RDA) AND CONTAINS SUCROSE OVER 5%, WITHOUT CONTENT OF ANIMAL ORIGIN OTHER PACKAGING, IN NON-AEROSOL PACKAGING: AQUADETRIM(R)VITAMIN D3 HYDROGEN SOLUTION FOR ORAL USE, 15,000 IU/ML IN 10ML VIAL WITH DROPPER DISPENSER; 1 VIAL IN CARDBOARD PACKAGE. ACTIVE INGREDIENT: 1ML (APPROXIMATELY 30 DROPS) SOLUTION CONTAINS: CHOLECALCIPHEROL 15000 IU (1 DROP CONTAINS APPROXIMATELY 500 IU VITAMIN D3). SERIES: 010323 - 24600 UP. EXPIRY DATE - 01.03.2026 UA/9205/01/01 29.03.2021 - UNLIMITED. TRADEMARK: AQUADETRIM. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A. MEDANA DEPARTMENT IN SIERADZ, POLAND COUNTRY OF PRODUCTION: POLAND(PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
|
POLAND | UKRAINE | 0 |
| 3004900000 | 1. MEDICINES (DRUGS FOR HUMANS) PACKAGED FOR RETAIL TRADE IN AEROSOL PACKAGING: ETORA, FILM-COATED TABLETS OF 120 MG, 7 TABLETS IN A BLISTER, 1 BLISTER IN A CARDBOARD BOX CHOVINA: 1 TABLET CONTAINS 120 MG ETORICOXIB. SERIES: P2403165 - 14000 EXP. EXPIRY DATE - 01.12.2027 UA/18682/01/03 13.04.2021 - 13.04.2026. TRADEMARK: MANUFACTURER: RONTIS HELLAS MEDICAL AND PHARMACEUTICALS .A., GREECE. COUNTRY OF PRODUCTION - GREECE (GR). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
|
GREECE | UKRAINE | 0 |
| 3004900000 | 1. MEDICINES (DRUGS FOR HUMANS) PACKAGED FOR RETAIL TRADE IN AEROSOL PACKAGING: VANATEX COMBI, FILM-COVERED TABLETS, 80MG/12.5MGPO 14 TABLETS IN A BLISTER; 2 BLISTERS IN A CARTON BOXES. ACTIVE INGREDIENT: 1 TABLET, WITH FILM COVER, CONTAINS 80MG VALSARTAN AND 12.5MG HYDROCHLOROTHIAZIDE. SERIES: 10224 - 25823 PACK. EXPIRY DATE - 01.02.2027 UA/12839/01/02 21.03.18- UNLIMITED. TRADEMARK: VANATEKS COMBI. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A., POLAND. BOBOTIK, ORAL DROPS, EMULSION, 66.66 MG/ML; 30 ML EACH IN A VIAL WITH A STOPPER-DROPPER AND A LID; 1 BOTTLE IN A CARDBOARD BOX. ACTIVE INGREDIENT: 1 ML OF EMULSION CONTAINS SIMETHICONE (DIMETHICONE, ACTIVATED WITH SILICON DIOXIDE IN THE FORM OF 30% EMULSION) 66.66 MG; 1ML CONTAINS APPROXIMATELY 27 DROPS. SERIES: 041123 - 11178 UP. EXPIRY DATE - 01.11.2026 RP UA/11716/01/01 02.07.21 - UNLIMITED TRADEMARK: BOBOTIK. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A. MEDANA DEPARTMENT IN SIERADZ, POLANDESPIRO, FILM-COATED TABLETS, 25 MG, 10 TABLETS IN BLISTERS, 3 BLISTERS IN CARDBOARD BOX #30. ACTIVE INGREDIENT: 1 FILM-COATED TABLET CONTAINS 25 MG EPLERENONE. SERIES: 51023 - 7380 EXP. EXPIRY DATE - 01.10.2027 UA/18267/01/01 25.08.20 - 25.08.25 TRADEMARK: ESPIRO. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A., POLAND. INDAPEN, COATED TABLETS, 2.5 MG OF 10 TABLETS IN BLISTERS; 3 BLISTERS IN CARDBOARD BOX NO. 30. ACTIVE INGREDIENT: 1 COATED TABLET CONTAINS 2.5 MGINDAPAMID. SERIES: 10224 - 10000 PCS. EXPIRY DATE - 01.02.2027UA/0877/01/01 17.05.19 - UNLIMITED. TRADEMARK: INDAPEN. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A., POLAND. PYRANTELPOLPHARMA, ORAL SUSPENSION, 250 MG/5 ML OF 15 ML IN A VIAL, 1 VIAL WITH A DRILL IN A CARDBOARD BOX. ACTIVE INGREDIENT: 5 ML OF SUSPENSION CONTAINS PYRANTEL (AS PYRANTEL PAMOATE) 250 MG. SERIES: 020124 - 19440 UP. EXPIRY DATE - 01.01.2027 UA/9225/01/01 31.10.19 - UNLIMITED. TRADEMARK: PYRANTEL POLPHARMA. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A. MEDANA DEPARTMENT IN SIERADZ, POLAND LINEFOR, HARD CAPSULES OF 75 MG; 14 CAPSULES IN BLISTERS; 4 BLISTERS IN A CARDBOARD BOX NO. 56. ACTIVE INGREDIENT: 1 CAPSULE CONTAINS PREGABALIN 75 MG. SERIES: 60923 - 3490 UNITS. EXPIRY DATE - 09/01/2026 UA/18144/01/01 06/15/2020- 06/15/2025 TRADEMARK: LINEFOR. MANUFACTURER: PHARMACEUTICAL PLANT """"POLPHARMA"""" S.A., POLAND. COUNTRY OF PRODUCTION - POLAND (PL). LABELING IS PRESENT AND CORRESPONDS TO STANDARDS ESTABLISHED BY LEGISLATION | |
|
POLAND | UKRAINE | 0 |
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