Inke S.A: APIs manufacturing plant.
01 1Inke, S.A. Castellbisbal ES
02 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
05 1CAMBREX CHARLES CITY, INC. Charles City US
06 1CIPLA LIMITED Mumbai IN
07 1GEDEON RICHTER PLC Budapest HU
08 1HIKAL LIMITED Bangalore IN
09 1HIKMA PHARMACEUTICALS CO. LTD. Amman JO
10 1IPCA Laboratories Limited Mumbai IN
11 1NATCO PHARMA LIMITED Hyderabad IN
12 1QILU PHARMACEUTICAL CO., LTD. Jinan CN
13 1SHODHANA LABORATORIES PRIVATE LIMITED Jeedimetla IN
14 1SMS PHARMACEUTICALS LIMITED Hyderabad IN
15 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
16 1SYMED LABS LIMITED Hyderabad IN
17 1TARO PHARMACEUTICAL INDUSTRIES, LTD. Haifa Bay IL
18 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
Inke S.A: APIs manufacturing plant.
Ondansetron Hydrochloride Dihydrate
Certificate Number : R1-CEP 2005-056 - Rev 00
Status : Valid
Issue Date : 2012-05-24
Type : Chemical
Substance Number : 2016
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Ondansetron Hydrochloride Dihydrate
Certificate Number : R1-CEP 2005-071 - Rev 06
Status : Valid
Issue Date : 2023-05-23
Type : Chemical
Substance Number : 2016
A Ondansetron Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ondansetron Hydrochloride, including repackagers and relabelers. The FDA regulates Ondansetron Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ondansetron Hydrochloride 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 Ondansetron Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ondansetron Hydrochloride supplier is an individual or a company that provides Ondansetron Hydrochloride active pharmaceutical ingredient (API) or Ondansetron Hydrochloride finished formulations upon request. The Ondansetron Hydrochloride suppliers may include Ondansetron Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ondansetron Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ondansetron Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Ondansetron Hydrochloride Certificate of Suitability (COS). The purpose of a Ondansetron Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ondansetron Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ondansetron Hydrochloride to their clients by showing that a Ondansetron Hydrochloride CEP has been issued for it. The manufacturer submits a Ondansetron Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ondansetron Hydrochloride CEP holder for the record. Additionally, the data presented in the Ondansetron Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ondansetron Hydrochloride DMF.
A Ondansetron Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ondansetron Hydrochloride 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 Ondansetron Hydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 18 companies offering Ondansetron Hydrochloride
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