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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

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PharmaCompass
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

CEP 2013-073 - Rev 04
Valid
Chemical
2024-11-19
2270
Polpharma CB

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma 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 CB
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

R1-CEP 2013-072 - Rev 02
Valid
Chemical
2022-03-14
2270
Polpharma CB

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

Sildenafil Citrate, Process A

Certificate Number : R1-CEP 2013-072 - Rev 02

Status : Valid

Issue Date : 2022-03-14

Type : Chemical

Substance Number : 2270

Polpharma CB

Sildenafil Citrate Manufacturers

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.

Sildenafil Citrate Suppliers

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.

Sildenafil Citrate CEP

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.

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.