Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 1GRANULES INDIA LIMITED Hyderabad IN
02 1Moehs Iberica S.L. Rubi ES
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1AREVIPHARMA GMBH Radebeul DE
05 1CTX LIFESCIENCES PVT. LIMITED Surat IN
06 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
07 1ESTEVE QUIMICA S.A. Barcelona ES
08 1HEC PHARM CO., LTD. Yidu City CN
09 1IPCA LABORATORIES LIMITED Mumbai IN
10 1MSN LIFE SCIENCES PRIVATE LIMITED Bhiknoor Village IN
11 1POLYDRUG LABORATORIES PVT. LTD. Mumbai IN
12 1SANECA PHARMACEUTICALS A.S. Hlohovec SK
13 2SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
14 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
15 1ZAKŁADY FARMACEUTYCZNE POLPHARMA S.A. Starogard Gdański PL
16 1ZHEJIANG APELOA JIAYUAN PHARMACEUTICAL CO., LTD. Dongyang City CN
17 1ZHEJIANG HISOAR CHUANNAN PHARMACEUTICAL CO., LTD. Taizhou City CN
18 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Certificate Number : CEP 2019-232 - Rev 02
Status : Valid
Issue Date : 2024-06-10
Type : Chemical
Substance Number : 1448
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : CEP 2004-202 - Rev 07
Status : Valid
Issue Date : 2024-02-27
Type : Chemical
Substance Number : 1448
A Metoprolol Succinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metoprolol Succinate, including repackagers and relabelers. The FDA regulates Metoprolol Succinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metoprolol Succinate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Metoprolol Succinate supplier is an individual or a company that provides Metoprolol Succinate active pharmaceutical ingredient (API) or Metoprolol Succinate finished formulations upon request. The Metoprolol Succinate suppliers may include Metoprolol Succinate API manufacturers, exporters, distributors and traders.
click here to find a list of Metoprolol Succinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Metoprolol Succinate CEP of the European Pharmacopoeia monograph is often referred to as a Metoprolol Succinate Certificate of Suitability (COS). The purpose of a Metoprolol Succinate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Metoprolol Succinate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Metoprolol Succinate to their clients by showing that a Metoprolol Succinate CEP has been issued for it. The manufacturer submits a Metoprolol Succinate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Metoprolol Succinate CEP holder for the record. Additionally, the data presented in the Metoprolol Succinate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Metoprolol Succinate DMF.
A Metoprolol Succinate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Metoprolol Succinate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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