01 1GADOR S.A. Pilar AR
02 1GEDEON RICHTER PLC. Budapest HU
03 1INDUSTRIALE CHIMICA S.R.L. Saronno IT
04 3STERLING S.p.A. Solomeo Di Corciano IT
01 4Norgestimate
02 1Norgestimate, Optimised process SM-ROS-2, code 200448
03 1Norgestimate, Optimized process
01 1Argentina
02 1Hungary
03 4Italy
01 1Expired
02 5Valid
Certificate Number : R0-CEP 2010-012 - Rev 00
Status : Expired
Issue Date : 2011-11-17
Type : Chemical
Substance Number : 1732
Certificate Number : R1-CEP 2009-125 - Rev 01
Status : Valid
Issue Date : 2021-12-02
Type : Chemical
Substance Number : 1732
Certificate Number : CEP 2017-189 - Rev 01
Status : Valid
Issue Date : 2023-09-28
Type : Chemical
Substance Number : 1732
Norgestimate, Optimized Process
Certificate Number : R0-CEP 2021-049 - Rev 02
Status : Valid
Issue Date : 2022-10-10
Type : Chemical
Substance Number : 1732
Certificate Number : R1-CEP 2009-305 - Rev 00
Status : Valid
Issue Date : 2016-11-29
Type : Chemical
Substance Number : 1732
Norgestimate, Optimised Process SM-ROS-2, Code 2...
Certificate Number : CEP 2023-354 - Rev 00
Status : Valid
Issue Date : 2024-02-16
Type : Chemical
Substance Number : 1732
41
PharmaCompass offers a list of Norgestimate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Norgestimate manufacturer or Norgestimate supplier for your needs.
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PharmaCompass also assists you with knowing the Norgestimate API Price utilized in the formulation of products. Norgestimate API Price is not always fixed or binding as the Norgestimate Price is obtained through a variety of data sources. The Norgestimate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CID6540478 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CID6540478, including repackagers and relabelers. The FDA regulates CID6540478 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CID6540478 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A CID6540478 supplier is an individual or a company that provides CID6540478 active pharmaceutical ingredient (API) or CID6540478 finished formulations upon request. The CID6540478 suppliers may include CID6540478 API manufacturers, exporters, distributors and traders.
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A CID6540478 CEP of the European Pharmacopoeia monograph is often referred to as a CID6540478 Certificate of Suitability (COS). The purpose of a CID6540478 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CID6540478 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CID6540478 to their clients by showing that a CID6540478 CEP has been issued for it. The manufacturer submits a CID6540478 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CID6540478 CEP holder for the record. Additionally, the data presented in the CID6540478 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CID6540478 DMF.
A CID6540478 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CID6540478 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 CID6540478 suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering CID6540478
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