Inke S.A: APIs manufacturing plant.

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01 1INKE, S.A. Castellbisbal ES
02 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
03 1TAPI NL B.V. Amsterdam NL
04 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
05 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
06 1CAMBREX CHARLES CITY, INC. Charles City US
07 1CIPLA LIMITED Mumbai IN
08 1GEDEON RICHTER PLC. Budapest HU
09 1HIKAL LIMITED Bangalore IN
10 1HIKMA PHARMACEUTICALS CO. LTD. Amman JO
11 1IPCA Laboratories Limited Mumbai IN
12 1NATCO PHARMA LIMITED Hyderabad IN
13 1QILU PHARMACEUTICAL CO., LTD. Jinan CN
14 1SHODHANA LABORATORIES PRIVATE LIMITED Jeedimetla IN
15 1SMS PHARMACEUTICALS LIMITED Hyderabad IN
16 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
17 1SYMED LABS LIMITED Hyderabad IN
18 1TARO PHARMACEUTICAL INDUSTRIES, LTD. Haifa Bay IL
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01 18Ondansetron hydrochloride dihydrate
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01 1China
02 1Hungary
03 11India
04 2Israel
05 1Jordan
06 1Spain
07 1U.S.A
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01 2Expired
02 16Valid
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.
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
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Ondansetron Hydrochloride Dihydrate
Certificate Number : CEP 2004-042 - Rev 04
Status : Valid
Issue Date : 2026-04-09
Type : Chemical
Substance Number : 2016
Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
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Ondansetron Hydrochloride Dihydrate
Certificate Number : CEP 2007-012 - Rev 06
Status : Valid
Issue Date : 2024-02-28
Type : Chemical
Substance Number : 2016

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Ondansetron Hydrochloride Dihydrate
Certificate Number : R1-CEP 2003-053 - Rev 01
Status : Valid
Issue Date : 2011-08-22
Type : Chemical
Substance Number : 2016

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Ondansetron Hydrochloride Dihydrate
Certificate Number : R1-CEP 2007-237 - Rev 02
Status : Valid
Issue Date : 2019-09-18
Type : Chemical
Substance Number : 2016

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Ondansetron Hydrochloride Dihydrate
Certificate Number : R1-CEP 2009-114 - Rev 01
Status : Valid
Issue Date : 2023-05-04
Type : Chemical
Substance Number : 2016

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Ondansetron Hydrochloride Dihydrate
Certificate Number : R1-CEP 2009-319 - Rev 04
Status : Valid
Issue Date : 2019-09-16
Type : Chemical
Substance Number : 2016

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Ondansetron Hydrochloride Dihydrate
Certificate Number : R1-CEP 2004-066 - Rev 04
Status : Valid
Issue Date : 2022-08-17
Type : Chemical
Substance Number : 2016

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Ondansetron Hydrochloride Dihydrate
Certificate Number : R0-CEP 2019-252 - Rev 00
Status : Valid
Issue Date : 2021-12-06
Type : Chemical
Substance Number : 2016

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PharmaCompass offers a list of Ondansetron Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Ondansetron Hydrochloride manufacturer or Ondansetron Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ondansetron Hydrochloride manufacturer or Ondansetron Hydrochloride supplier.
A Zensana manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zensana, including repackagers and relabelers. The FDA regulates Zensana manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zensana 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 Zensana manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Zensana supplier is an individual or a company that provides Zensana active pharmaceutical ingredient (API) or Zensana finished formulations upon request. The Zensana suppliers may include Zensana API manufacturers, exporters, distributors and traders.
click here to find a list of Zensana suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Zensana CEP of the European Pharmacopoeia monograph is often referred to as a Zensana Certificate of Suitability (COS). The purpose of a Zensana CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Zensana EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Zensana to their clients by showing that a Zensana CEP has been issued for it. The manufacturer submits a Zensana CEP (COS) as part of the market authorization procedure, and it takes on the role of a Zensana CEP holder for the record. Additionally, the data presented in the Zensana CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Zensana DMF.
A Zensana CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Zensana 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 Zensana suppliers with CEP (COS) on PharmaCompass.
We have 18 companies offering Zensana
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