Aspen API. More than just an API™
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
Aspen API. More than just an API™
Aspen API. More than just an API™
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
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PharmaCompass offers a list of Norethisterone 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 Norethisterone Acetate manufacturer or Norethisterone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Norethisterone Acetate manufacturer or Norethisterone Acetate supplier.
PharmaCompass also assists you with knowing the Norethisterone Acetate API Price utilized in the formulation of products. Norethisterone Acetate API Price is not always fixed or binding as the Norethisterone Acetate Price is obtained through a variety of data sources. The Norethisterone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ENTA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ENTA, including repackagers and relabelers. The FDA regulates ENTA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ENTA 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 ENTA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ENTA supplier is an individual or a company that provides ENTA active pharmaceutical ingredient (API) or ENTA finished formulations upon request. The ENTA suppliers may include ENTA API manufacturers, exporters, distributors and traders.
click here to find a list of ENTA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ENTA CEP of the European Pharmacopoeia monograph is often referred to as a ENTA Certificate of Suitability (COS). The purpose of a ENTA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ENTA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ENTA to their clients by showing that a ENTA CEP has been issued for it. The manufacturer submits a ENTA CEP (COS) as part of the market authorization procedure, and it takes on the role of a ENTA CEP holder for the record. Additionally, the data presented in the ENTA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ENTA DMF.
A ENTA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ENTA 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 ENTA suppliers with CEP (COS) on PharmaCompass.
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