Inke S.A: APIs manufacturing plant.
01 1Inke, S.A. Castellbisbal ES
02 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
03 1Medichem, S.A. Sant Joan Despí ES
04 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
05 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
06 1CIPLA LIMITED Mumbai IN
07 1JANSSEN PHARMACEUTICA NV Beerse BE
08 2JUBILANT PHARMOVA LIMITED Nanjangud IN
09 1Janssen Pharmaceutical Ltd County Cork IE
10 1LUPIN LIMITED Mumbai IN
11 1RPG Life Sciences Limited Navi Mumbai IN
12 1SYNTHON B.V. Nijmegen NL
13 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
14 1TORRENT PHARMACEUTICALS LIMITED Ahmedabad IN
15 1VENKATA NARAYANA ACTIVE INGREDIENTS PRIVATE LIMITED Chennai IN
16 1WUXI JIDA PHARMACEUTICAL CO., LTD. Jiangyin CN
17 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
18 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
Inke S.A: APIs manufacturing plant.
Certificate Number : R1-CEP 2006-054 - Rev 00
Status : Valid
Issue Date : 2012-07-16
Type : Chemical
Substance Number : 1559
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Certificate Number : R1-CEP 2009-243 - Rev 03
Status : Valid
Issue Date : 2023-07-17
Type : Chemical
Substance Number : 1559
Medichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.
Certificate Number : R1-CEP 2007-105 - Rev 00
Status : Valid
Issue Date : 2013-04-30
Type : Chemical
Substance Number : 1559
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : R1-CEP 2003-110 - Rev 05
Status : Valid
Issue Date : 2023-05-02
Type : Chemical
Substance Number : 1559
A Risperdal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Risperdal, including repackagers and relabelers. The FDA regulates Risperdal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Risperdal 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 Risperdal manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Risperdal supplier is an individual or a company that provides Risperdal active pharmaceutical ingredient (API) or Risperdal finished formulations upon request. The Risperdal suppliers may include Risperdal API manufacturers, exporters, distributors and traders.
click here to find a list of Risperdal suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Risperdal CEP of the European Pharmacopoeia monograph is often referred to as a Risperdal Certificate of Suitability (COS). The purpose of a Risperdal CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Risperdal EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Risperdal to their clients by showing that a Risperdal CEP has been issued for it. The manufacturer submits a Risperdal CEP (COS) as part of the market authorization procedure, and it takes on the role of a Risperdal CEP holder for the record. Additionally, the data presented in the Risperdal CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Risperdal DMF.
A Risperdal CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Risperdal 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 Risperdal suppliers with CEP (COS) on PharmaCompass.
We have 17 companies offering Risperdal
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