Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1PHARMACEUTICAL WORKS POLPHARMA S.A. Starogard Gdanski PL
02 1ZAKŁADY FARMACEUTYCZNE POLPHARMA S.A. Starogard Gdański PL
03 1AMOLI ORGANICS PRIVATE LIMITED Mumbai IN
04 1ANDHRA ORGANICS LIMITED Pydibhimavaram Village IN
05 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
06 1AZICO BIOPHORE INDIA PRIVATE LIMITED Hyderabad IN
07 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
08 1HETERO DRUGS LIMITED Hyderabad IN
09 1JINAN MINGXIN PHARMACEUTICAL CO., LTD. Zhangqiu City CN
10 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
11 1MAPRIMED S.A. Buenos Aires AR
12 1MSN ORGANICS PRIVATE LIMITED Bibinagar Village IN
13 1PHALANX LABS PRIVATE LIMITED Hyderabad IN
14 1RAKS PHARMA PVT. LTD. Visakhapatnam IN
15 1RAKSHIT PHARMACEUTICALS LIMITED Anakapalli IN
16 1SICHUAN KELUN PHARMACEUTICAL CO., LTD. Qionglai CN
17 1SMS LIFESCIENCES INDIA LIMITED Hyderabad IN
18 1SMS PHARMACEUTICALS LIMITED Hyderabad IN
19 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
20 1TORRENT PHARMACEUTICALS LIMITED Ahmedabad IN
21 1Zhejiang Jiuzhou Pharmaceutical Co., Ltd. Taizhou City CN
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Sildenafil Citrate, Process B, Standard, Milled ...
Certificate Number : CEP 2013-073 - Rev 04
Status : Valid
Issue Date : 2024-11-19
Type : Chemical
Substance Number : 2270
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Certificate Number : R1-CEP 2013-072 - Rev 02
Status : Valid
Issue Date : 2022-03-14
Type : Chemical
Substance Number : 2270
A Sildenafil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sildenafil, including repackagers and relabelers. The FDA regulates Sildenafil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sildenafil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Sildenafil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sildenafil supplier is an individual or a company that provides Sildenafil active pharmaceutical ingredient (API) or Sildenafil finished formulations upon request. The Sildenafil suppliers may include Sildenafil API manufacturers, exporters, distributors and traders.
click here to find a list of Sildenafil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sildenafil CEP of the European Pharmacopoeia monograph is often referred to as a Sildenafil Certificate of Suitability (COS). The purpose of a Sildenafil CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sildenafil EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sildenafil to their clients by showing that a Sildenafil CEP has been issued for it. The manufacturer submits a Sildenafil CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sildenafil CEP holder for the record. Additionally, the data presented in the Sildenafil CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sildenafil DMF.
A Sildenafil CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sildenafil CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Sildenafil suppliers with CEP (COS) on PharmaCompass.
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