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01 1ASPEN OSS B.V. Oss NL
02 1BAYER AG Leverkusen DE
03 1GEDEON RICHTER PLC Budapest HU
04 1VALDEPHARM Val de Reuil FR
01 3Norethisterone acetate
02 1Norethisterone acetate, micronised, non-micronised
01 1France
02 1Germany
03 1Hungary
04 1Netherlands
01 4Valid
Certificate Number : R1-CEP 1996-042 - Rev 07
Status : Valid
Issue Date : 2022-11-25
Type : Chemical
Substance Number : 850
Certificate Number : R1-CEP 2000-111 - Rev 04
Status : Valid
Issue Date : 2017-06-22
Type : Chemical
Substance Number : 850
Norethisterone Acetate, Micronised, Non-micronis...
Certificate Number : R1-CEP 2011-242 - Rev 02
Status : Valid
Issue Date : 2023-04-03
Type : Chemical
Substance Number : 850
Certificate Number : CEP 2021-402 - Rev 01
Status : Valid
Issue Date : 2024-11-25
Type : Chemical
Substance Number : 850
A Norethisterone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Norethisterone Acetate, including repackagers and relabelers. The FDA regulates Norethisterone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Norethisterone Acetate 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 Norethisterone Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Norethisterone Acetate supplier is an individual or a company that provides Norethisterone Acetate active pharmaceutical ingredient (API) or Norethisterone Acetate finished formulations upon request. The Norethisterone Acetate suppliers may include Norethisterone Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Norethisterone Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Norethisterone Acetate CEP of the European Pharmacopoeia monograph is often referred to as a Norethisterone Acetate Certificate of Suitability (COS). The purpose of a Norethisterone Acetate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Norethisterone Acetate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Norethisterone Acetate to their clients by showing that a Norethisterone Acetate CEP has been issued for it. The manufacturer submits a Norethisterone Acetate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Norethisterone Acetate CEP holder for the record. Additionally, the data presented in the Norethisterone Acetate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Norethisterone Acetate DMF.
A Norethisterone Acetate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Norethisterone Acetate 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 Norethisterone Acetate suppliers with CEP (COS) on PharmaCompass.
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