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
01 19Sildenafil citrate
02 1Sildenafil citrate, Process A
03 1Sildenafil citrate, Process B, standard, milled and micronised
01 1Argentina
02 3China
03 15India
04 2Poland
01 2Expired
02 18Valid
03 1Withdrawn by Holder
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
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.
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
Certificate Number : R1-CEP 2014-223 - Rev 01
Status : Valid
Issue Date : 2021-02-04
Type : Chemical
Substance Number : 2270
Certificate Number : CEP 2022-251 - Rev 00
Status : Valid
Issue Date : 2024-03-06
Type : Chemical
Substance Number : 2270
Certificate Number : R1-CEP 2013-291 - Rev 00
Status : Valid
Issue Date : 2019-12-16
Type : Chemical
Substance Number : 2270
Certificate Number : R1-CEP 2014-246 - Rev 00
Status : Valid
Issue Date : 2021-01-18
Type : Chemical
Substance Number : 2270
Certificate Number : R1-CEP 2014-361 - Rev 01
Status : Valid
Issue Date : 2023-01-10
Type : Chemical
Substance Number : 2270
Certificate Number : R1-CEP 2013-060 - Rev 00
Status : Valid
Issue Date : 2020-01-14
Type : Chemical
Substance Number : 2270
Certificate Number : CEP 2012-317 - Rev 01
Status : Valid
Issue Date : 2024-07-25
Type : Chemical
Substance Number : 2270
Certificate Number : CEP 2013-346 - Rev 02
Status : Valid
Issue Date : 2024-10-04
Type : Chemical
Substance Number : 2270
A Sildenafil Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sildenafil Citrate, including repackagers and relabelers. The FDA regulates Sildenafil Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sildenafil Citrate 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 Citrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sildenafil Citrate supplier is an individual or a company that provides Sildenafil Citrate active pharmaceutical ingredient (API) or Sildenafil Citrate finished formulations upon request. The Sildenafil Citrate suppliers may include Sildenafil Citrate API manufacturers, exporters, distributors and traders.
click here to find a list of Sildenafil Citrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sildenafil Citrate CEP of the European Pharmacopoeia monograph is often referred to as a Sildenafil Citrate Certificate of Suitability (COS). The purpose of a Sildenafil Citrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sildenafil Citrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sildenafil Citrate to their clients by showing that a Sildenafil Citrate CEP has been issued for it. The manufacturer submits a Sildenafil Citrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sildenafil Citrate CEP holder for the record. Additionally, the data presented in the Sildenafil Citrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sildenafil Citrate DMF.
A Sildenafil Citrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sildenafil Citrate 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 Citrate suppliers with CEP (COS) on PharmaCompass.
We have 20 companies offering Sildenafil Citrate
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