Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1ZAKŁADY FARMACEUTYCZNE POLPHARMA S.A. Starogard Gdański PL
02 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
03 1USV PRIVATE LIMITED Mumbai IN
04 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
05 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
06 1CTX LIFESCIENCES PVT. LIMITED Surat IN
07 1Changzhou Pharmaceutical Factory Changzhou CN
08 1DIVI'S LABORATORIES LIMITED Hyderabad IN
09 1GLENMARK LIFE SCIENCES LIMITED Mumbai IN
10 1HONOUR LAB LIMITED Hyderabad IN
11 1INTAS PHARMACEUTICALS LIMITED Ahmedabad IN
12 1Jiangxi Synergy Pharmaceutical Co., Ltd. Fengxin CN
13 1KRKA, d.d., Novo mesto Novo mesto SI
14 1LEE PHARMA LIMITED Hyderabad IN
15 1MANKIND PHARMA LIMITED New Delhi IN
16 1MICRO LABS LIMITED Bengaluru IN
17 2MSN ORGANICS PRIVATE LIMITED Bibinagar Village IN
18 1PHARMARESOURCES (KAIYUAN) COMPANY LIMITED Kaiyuan City CN
19 1SHAOXING JINGXIN PHARMACEUTICAL CO., LTD. Shangyu CN
20 1SHENZHEN SALUBRIS PHARMACEUTICALS CO., LTD. Shenzhen City CN
21 1SUZHOU LIXIN PHARMACEUTICAL CO., LTD. Suzhou CN
22 1VIYASH LIFE SCIENCES PRIVATE LIMITED Hyderabad IN
23 1ZHEJIANG AUSUN PHARMACEUTICAL CO., LTD. Taizhou CN
24 1ZHEJIANG JIANGBEI NANHAI PHARMACEUTICAL CO., LTD Linhai City CN
25 1ZHEJIANG TIANYU PHARMACEUTICAL CO., LTD. Taizhou City CN
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Ticagrelor, Standard, Micronised
Certificate Number : CEP 2020-338 - Rev 02
Status : Valid
Issue Date : 2024-08-23
Type : Chemical
Substance Number : 3087
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Certificate Number : CEP 2020-331 - Rev 00
Status : Valid
Issue Date : 2023-11-28
Type : Chemical
Substance Number : 3087
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
Certificate Number : CEP 2023-128 - Rev 00
Status : Valid
Issue Date : 2024-07-04
Type : Chemical
Substance Number : 3087
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 2021-225 - Rev 00
Status : Valid
Issue Date : 2023-11-23
Type : Chemical
Substance Number : 3087
A Brilinta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Brilinta, including repackagers and relabelers. The FDA regulates Brilinta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Brilinta 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 Brilinta manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Brilinta supplier is an individual or a company that provides Brilinta active pharmaceutical ingredient (API) or Brilinta finished formulations upon request. The Brilinta suppliers may include Brilinta API manufacturers, exporters, distributors and traders.
click here to find a list of Brilinta suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Brilinta CEP of the European Pharmacopoeia monograph is often referred to as a Brilinta Certificate of Suitability (COS). The purpose of a Brilinta CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Brilinta EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Brilinta to their clients by showing that a Brilinta CEP has been issued for it. The manufacturer submits a Brilinta CEP (COS) as part of the market authorization procedure, and it takes on the role of a Brilinta CEP holder for the record. Additionally, the data presented in the Brilinta CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Brilinta DMF.
A Brilinta CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Brilinta 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 Brilinta suppliers with CEP (COS) on PharmaCompass.
We have 25 companies offering Brilinta
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
