Inke S.A: APIs manufacturing plant.
01 1Inke, S.A. Castellbisbal ES
02 1CORAL DRUGS PRIVATE LIMITED New Delhi IN
03 1Vamsi Labs Limited Solapur IN
04 1Farmabios SpA Gropello Cairoli IT
05 1FERMION OY Espoo FI
06 1AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN
07 1CIPLA LIMITED Mumbai IN
08 1Industriale Chimica S.R.L. Saronno IT
09 2LUSOCHIMICA S.P.A. Lomagna IT
10 1MELODY HEALTHCARE PVT. LTD. Mumbai IN
11 1MSN LABORATORIES PRIVATE LIMITED Rudraram Village IN
12 1MYLAN LABORATORIES LIMITED Hyderabad IN
13 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
Inke S.A: APIs manufacturing plant.
Certificate Number : R1-CEP 2006-024 - Rev 02
Status : Valid
Issue Date : 2020-10-15
Type : Chemical
Substance Number : 1724
Coral's API range includes Corticosteroids, Antihistamines. Hormones and Antineoplastics.
Certificate Number : R1-CEP 2016-105 - Rev 00
Status : Valid
Issue Date : 2022-09-28
Type : Chemical
Substance Number : 1724
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
Certificate Number : R1-CEP 2006-227 - Rev 02
Status : Valid
Issue Date : 2022-07-28
Type : Chemical
Substance Number : 1724
Axplora- The partner of choice for complex APIs.
Formoterol Fumarate Dihydrate, Micronised
Certificate Number : R1-CEP 2010-132 - Rev 01
Status : Valid
Issue Date : 2017-08-11
Type : Chemical
Substance Number : 1724
With Fermion, start the journey of your innovative API.
Formoterol Fumarate Dihydrate, Micronised
Certificate Number : CEP 2015-215 - Rev 02
Status : Valid
Issue Date : 2023-09-04
Type : Chemical
Substance Number : 1724
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Certificate Number : R1-CEP 2013-220 - Rev 02
Status : Valid
Issue Date : 2022-10-20
Type : Chemical
Substance Number : 1724
A Formoterol Fumarate Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Formoterol Fumarate Dihydrate, including repackagers and relabelers. The FDA regulates Formoterol Fumarate Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Formoterol Fumarate Dihydrate 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 Formoterol Fumarate Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Formoterol Fumarate Dihydrate supplier is an individual or a company that provides Formoterol Fumarate Dihydrate active pharmaceutical ingredient (API) or Formoterol Fumarate Dihydrate finished formulations upon request. The Formoterol Fumarate Dihydrate suppliers may include Formoterol Fumarate Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Formoterol Fumarate Dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Formoterol Fumarate Dihydrate CEP of the European Pharmacopoeia monograph is often referred to as a Formoterol Fumarate Dihydrate Certificate of Suitability (COS). The purpose of a Formoterol Fumarate Dihydrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Formoterol Fumarate Dihydrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Formoterol Fumarate Dihydrate to their clients by showing that a Formoterol Fumarate Dihydrate CEP has been issued for it. The manufacturer submits a Formoterol Fumarate Dihydrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Formoterol Fumarate Dihydrate CEP holder for the record. Additionally, the data presented in the Formoterol Fumarate Dihydrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Formoterol Fumarate Dihydrate DMF.
A Formoterol Fumarate Dihydrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Formoterol Fumarate Dihydrate 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 Formoterol Fumarate Dihydrate suppliers with CEP (COS) on PharmaCompass.
We have 13 companies offering Formoterol Fumarate Dihydrate
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