TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1TAPI NL B.V. Amsterdam NL
02 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1AUROBINDO PHARMA LIMITED Hyderabad IN
05 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
06 1ESTEVE QUIMICA S.A. Barcelona ES
07 1Eli Lilly SA County Cork IE
08 1Erregierre S.p.A. San Paolo D'Argon IT
09 1GEDEON RICHTER PLC. Budapest HU
10 1IPCA LABORATORIES LIMITED Mumbai IN
11 1Lilly del Caribe, Inc - PR01 Carolina PR
12 1NOSCH LABS PRIVATE LIMITED Hyderabad IN
13 2OLON S.P.A. Rodano IT
14 1Ranbaxy Laboratories Limited Gurgaon IN
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 1997-042 - Rev 13
Status : Valid
Issue Date : 2025-12-10
Type : Chemical
Substance Number : 1104
60
PharmaCompass offers a list of Fluoxetine 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 Fluoxetine Hydrochloride manufacturer or Fluoxetine Hydrochloride supplier for your needs.
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A Tuneluz manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tuneluz, including repackagers and relabelers. The FDA regulates Tuneluz manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tuneluz 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 Tuneluz manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Tuneluz supplier is an individual or a company that provides Tuneluz active pharmaceutical ingredient (API) or Tuneluz finished formulations upon request. The Tuneluz suppliers may include Tuneluz API manufacturers, exporters, distributors and traders.
click here to find a list of Tuneluz suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Tuneluz CEP of the European Pharmacopoeia monograph is often referred to as a Tuneluz Certificate of Suitability (COS). The purpose of a Tuneluz CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tuneluz EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tuneluz to their clients by showing that a Tuneluz CEP has been issued for it. The manufacturer submits a Tuneluz CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tuneluz CEP holder for the record. Additionally, the data presented in the Tuneluz CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tuneluz DMF.
A Tuneluz CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tuneluz 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 Tuneluz suppliers with CEP (COS) on PharmaCompass.
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