EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1Aventis Pharma Manufacturing Pte Ltd Singapore SG
02 1Aventis Pharma SA Antony FR
03 1FERMION OY Espoo FI
04 1Cambrex Profarmaco Milano S.r.l. Paullo IT
05 1MICRO LABS LIMITED Bengaluru IN
06 1OLON S.P.A. Rodano IT
01 6Sodium cromoglicate
01 1Finland
02 1France
03 1India
04 1Italy
05 1Singapore
06 1U.S.A
01 5Valid
02 1Withdrawn by Holder
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Certificate Number : R1-CEP 2001-421 - Rev 03
Status : Valid
Issue Date : 2019-05-03
Type : Chemical
Substance Number : 562
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : R0-CEP 1999-199 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2004-10-06
Type : Chemical
Substance Number : 562
With Fermion, start the journey of your innovative API.
With Fermion, start the journey of your innovative API.
Certificate Number : R1-CEP 2013-136 - Rev 00
Status : Valid
Issue Date : 2021-02-11
Type : Chemical
Substance Number : 562
Certificate Number : CEP 2006-055 - Rev 03
Status : Valid
Issue Date : 2024-02-19
Type : Chemical
Substance Number : 562
Certificate Number : CEP 2023-048 - Rev 00
Status : Valid
Issue Date : 2024-08-12
Type : Chemical
Substance Number : 562
Certificate Number : CEP 1996-107 - Rev 13
Status : Valid
Issue Date : 2024-06-10
Type : Chemical
Substance Number : 562
A Cromolyn Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cromolyn Sodium, including repackagers and relabelers. The FDA regulates Cromolyn Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cromolyn Sodium 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 Cromolyn Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cromolyn Sodium supplier is an individual or a company that provides Cromolyn Sodium active pharmaceutical ingredient (API) or Cromolyn Sodium finished formulations upon request. The Cromolyn Sodium suppliers may include Cromolyn Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Cromolyn Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cromolyn Sodium CEP of the European Pharmacopoeia monograph is often referred to as a Cromolyn Sodium Certificate of Suitability (COS). The purpose of a Cromolyn Sodium CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cromolyn Sodium EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cromolyn Sodium to their clients by showing that a Cromolyn Sodium CEP has been issued for it. The manufacturer submits a Cromolyn Sodium CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cromolyn Sodium CEP holder for the record. Additionally, the data presented in the Cromolyn Sodium CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cromolyn Sodium DMF.
A Cromolyn Sodium CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cromolyn Sodium 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 Cromolyn Sodium suppliers with CEP (COS) on PharmaCompass.
We have 6 companies offering Cromolyn Sodium
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