01 1Industriale Chimica S.R.L. Saronno IT
02 1Monachem Monaco MC
03 1NEWCHEM S.p.A. Milano IT
04 2STERLING S.p.A. Solomeo Di Corciano IT
05 2TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
01 4Nomegestrol acetate
02 1Nomegestrol acetate, Codes: 204628, 204637
03 1Nomegestrol acetate, Nomac grade B
04 1Nomegestrol acetate, Nomac grade C
01 2Israel
02 4Italy
03 1Monaco
01 5Valid
02 2Withdrawn by Holder
Certificate Number : R0-CEP 2019-038 - Rev 01
Status : Valid
Issue Date : 2021-04-01
Type : Chemical
Substance Number : 1551
Certificate Number : R1-CEP 2000-221 - Rev 04
Status : Withdrawn by Holder
Issue Date : 2016-12-13
Type : Chemical
Substance Number : 1551
Certificate Number : R0-CEP 2020-084 - Rev 01
Status : Valid
Issue Date : 2023-07-24
Type : Chemical
Substance Number : 1551
Certificate Number : R1-CEP 2010-179 - Rev 00
Status : Valid
Issue Date : 2016-11-10
Type : Chemical
Substance Number : 1551
Nomegestrol Acetate, Codes: 204628, 204637
Certificate Number : R0-CEP 2019-241 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2020-03-17
Type : Chemical
Substance Number : 1551
Nomegestrol Acetate, Nomac Grade C
Certificate Number : R1-CEP 2015-266 - Rev 01
Status : Valid
Issue Date : 2021-12-20
Type : Chemical
Substance Number : 1551
Nomegestrol Acetate, Nomac Grade B
Certificate Number : CEP 2014-178 - Rev 05
Status : Valid
Issue Date : 2024-09-25
Type : Chemical
Substance Number : 1551
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PharmaCompass offers a list of Nomegestrol Acetate 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 Nomegestrol Acetate manufacturer or Nomegestrol Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Nomegestrol Acetate API Price utilized in the formulation of products. Nomegestrol Acetate API Price is not always fixed or binding as the Nomegestrol Acetate Price is obtained through a variety of data sources. The Nomegestrol Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lutenyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lutenyl, including repackagers and relabelers. The FDA regulates Lutenyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lutenyl 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 Lutenyl supplier is an individual or a company that provides Lutenyl active pharmaceutical ingredient (API) or Lutenyl finished formulations upon request. The Lutenyl suppliers may include Lutenyl API manufacturers, exporters, distributors and traders.
click here to find a list of Lutenyl suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lutenyl CEP of the European Pharmacopoeia monograph is often referred to as a Lutenyl Certificate of Suitability (COS). The purpose of a Lutenyl CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lutenyl EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lutenyl to their clients by showing that a Lutenyl CEP has been issued for it. The manufacturer submits a Lutenyl CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lutenyl CEP holder for the record. Additionally, the data presented in the Lutenyl CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lutenyl DMF.
A Lutenyl CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lutenyl CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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