DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
02 1TAPI NL B.V. Amsterdam NL
03 1HONOUR LAB LIMITED Hyderabad IN
04 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
05 1ALIVUS LIFE SCIENCES LIMITED Mumbai IN
06 1CTX LIFESCIENCES PVT. LIMITED Surat IN
07 1Changzhou Pharmaceutical Factory Changzhou CN
08 1DIVI'S LABORATORIES LIMITED Hyderabad IN
09 1INTAS PHARMACEUTICALS LIMITED Ahmedabad IN
10 1JIANGXI SYNERGY PHARMACEUTICAL CO., LTD. Yichun CN
11 1KRKA, d.d., Novo mesto Novo mesto SI
12 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
13 1MICRO LABS LIMITED Bengaluru IN
14 2MSN ORGANICS PRIVATE LIMITED Bibinagar Village IN
15 1PHARMARESOURCES (KAIYUAN) COMPANY LIMITED Kaiyuan City CN
16 1SHAOXING JINGXIN PHARMACEUTICAL CO., LTD. Shangyu CN
17 1SHENZHEN SALUBRIS PHARMACEUTICALS CO., LTD. Shenzhen City CN
18 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
19 1SUZHOU LIXIN PHARMACEUTICAL CO., LTD. Suzhou CN
20 1USV PRIVATE LIMITED Mumbai IN
21 1VIYASH LIFE SCIENCES PRIVATE LIMITED Hyderabad IN
22 1ZHEJIANG AUSUN PHARMACEUTICAL CO., LTD. Taizhou CN
23 1ZHEJIANG JIANGBEI NANHAI PHARMACEUTICAL CO., LTD Linhai City CN
24 1ZHEJIANG TIANYU PHARMACEUTICAL CO., LTD. Taizhou City CN
25 1Zhejiang Supor Pharmaceuticals Co., Ltd. Shaoxing CN
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
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 01
Status : Valid
Issue Date : 2025-06-27
Type : Chemical
Substance Number : 3087
Honour is a leading global CDMO and specialty chemicals manufacturer with seven world-class sites delivering quality-driven solutions.
Certificate Number : CEP 2022-131 - Rev 00
Status : Valid
Issue Date : 2024-11-18
Type : Chemical
Substance Number : 3087
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PharmaCompass offers a list of Ticagrelor API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Ticagrelor manufacturer or Ticagrelor supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ticagrelor manufacturer or Ticagrelor supplier.
PharmaCompass also assists you with knowing the Ticagrelor API Price utilized in the formulation of products. Ticagrelor API Price is not always fixed or binding as the Ticagrelor Price is obtained through a variety of data sources. The Ticagrelor Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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:
