DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
02 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 1APOTEX PHARMACHEM INDIA PVT. LTD Bangalore IN
04 1AURORE LIFE SCIENCES PRIVATE LIMITED Hyderabad IN
05 1EXCELLA GMBH Feucht DE
06 1Erregierre S.p.A. San Paolo D'Argon IT
07 2GLOCHEM INDUSTRIES PRIVATE LIMITED Hyderabad IN
08 1HETERO DRUGS LIMITED Hyderabad IN
09 1KYONGBO PHARMACEUTICAL CO., LTD. Asan-si KR
10 1MEDILUX LABORATORIES PRIVATE LIMITED Pithampur IN
11 1OLON S.P.A. Rodano IT
01 11Raloxifene hydrochloride
02 1Raloxifene hydrochloride, LAXAI
03 1Raloxifene hydrochloride, Modified process
01 1Canada
02 1Germany
03 8India
04 2Italy
05 1South Korea
01 1Expired
02 11Valid
03 1Withdrawn by Holder
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Certificate Number : R1-CEP 2014-054 - Rev 01
Status : Valid
Issue Date : 2023-03-31
Type : Chemical
Substance Number : 2375
Certificate Number : CEP 2017-097 - Rev 01
Status : Valid
Issue Date : 2024-08-22
Type : Chemical
Substance Number : 2375
Certificate Number : CEP 2012-016 - Rev 02
Status : Valid
Issue Date : 2024-01-05
Type : Chemical
Substance Number : 2375
Raloxifene Hydrochloride, Modified Process
Certificate Number : CEP 2024-069 - Rev 00
Status : Valid
Issue Date : 2024-04-24
Type : Chemical
Substance Number : 2375
Certificate Number : CEP 2022-165 - Rev 00
Status : Valid
Issue Date : 2024-04-22
Type : Chemical
Substance Number : 2375
Certificate Number : R1-CEP 2010-205 - Rev 00
Status : Valid
Issue Date : 2017-09-06
Type : Chemical
Substance Number : 2375
Certificate Number : R1-CEP 2010-227 - Rev 01
Status : Valid
Issue Date : 2019-10-15
Type : Chemical
Substance Number : 2375
Certificate Number : R1-CEP 2011-349 - Rev 00
Status : Valid
Issue Date : 2020-11-30
Type : Chemical
Substance Number : 2375
Certificate Number : CEP 2023-432 - Rev 00
Status : Valid
Issue Date : 2024-12-11
Type : Chemical
Substance Number : 2375
Certificate Number : R1-CEP 2015-171 - Rev 00
Status : Valid
Issue Date : 2022-04-08
Type : Chemical
Substance Number : 2375
A Evista manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Evista, including repackagers and relabelers. The FDA regulates Evista manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Evista 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 Evista manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Evista supplier is an individual or a company that provides Evista active pharmaceutical ingredient (API) or Evista finished formulations upon request. The Evista suppliers may include Evista API manufacturers, exporters, distributors and traders.
click here to find a list of Evista suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Evista CEP of the European Pharmacopoeia monograph is often referred to as a Evista Certificate of Suitability (COS). The purpose of a Evista CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Evista EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Evista to their clients by showing that a Evista CEP has been issued for it. The manufacturer submits a Evista CEP (COS) as part of the market authorization procedure, and it takes on the role of a Evista CEP holder for the record. Additionally, the data presented in the Evista CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Evista DMF.
A Evista CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Evista 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 Evista suppliers with CEP (COS) on PharmaCompass.
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