Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1SUPRIYA LIFESCIENCE LIMITED Mumbai IN
02 1QIDONG DONGYUE PHARMACEUTICAL CO., LTD. Qidong CN
03 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S.P.A. Milano IT
04 1WANBURY LIMITED Thane IN
01 4Diphenhydramine hydrochloride
01 1China
02 1India
03 1Italy
04 1Blank
01 4Valid
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Certificate Number : CEP 2019-120 - Rev 01
Status : Valid
Issue Date : 2025-02-13
Type : Chemical
Substance Number : 23
Certificate Number : CEP 2023-023 - Rev 00
Status : Valid
Issue Date : 2025-01-16
Type : Chemical
Substance Number : 23
Certificate Number : R1-CEP 2015-098 - Rev 00
Status : Valid
Issue Date : 2021-06-07
Type : Chemical
Substance Number : 23
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Certificate Number : CEP 2013-285 - Rev 01
Status : Valid
Issue Date : 2026-04-02
Type : Chemical
Substance Number : 23
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Diphenhydramine 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 Diphenhydramine Hydrochloride manufacturer or Diphenhydramine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diphenhydramine Hydrochloride manufacturer or Diphenhydramine Hydrochloride supplier.
A Cathejell manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cathejell, including repackagers and relabelers. The FDA regulates Cathejell manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cathejell 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 Cathejell manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Cathejell supplier is an individual or a company that provides Cathejell active pharmaceutical ingredient (API) or Cathejell finished formulations upon request. The Cathejell suppliers may include Cathejell API manufacturers, exporters, distributors and traders.
click here to find a list of Cathejell suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Cathejell CEP of the European Pharmacopoeia monograph is often referred to as a Cathejell Certificate of Suitability (COS). The purpose of a Cathejell CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cathejell EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cathejell to their clients by showing that a Cathejell CEP has been issued for it. The manufacturer submits a Cathejell CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cathejell CEP holder for the record. Additionally, the data presented in the Cathejell CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cathejell DMF.
A Cathejell CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cathejell 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 Cathejell suppliers with CEP (COS) on PharmaCompass.
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