Aspen API. More than just an API™
01 1Aspen Oss B.V.
02 1Bayer AG
03 1STERLING SPA
04 2Valdepharm
01 1NORETHINDRONE ACETATE
02 1Norethindrone Acetate
03 1Norethindrone acetate
04 1Norethindrone acetate micronized
05 1Norethisterone acetate
01 1Germany
02 1Italy
03 2Luxembourg
04 1Netherlands
Aspen API. More than just an API™
NDC Package Code : 60870-0236
Start Marketing Date : 1980-04-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12866-1014
Start Marketing Date : 2017-05-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 24823-908
Start Marketing Date : 2010-05-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 24823-909
Start Marketing Date : 2011-09-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64918-1404
Start Marketing Date : 2014-04-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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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 MINASTRIN 24 FE-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MINASTRIN 24 FE-1, including repackagers and relabelers. The FDA regulates MINASTRIN 24 FE-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MINASTRIN 24 FE-1 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 MINASTRIN 24 FE-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MINASTRIN 24 FE-1 supplier is an individual or a company that provides MINASTRIN 24 FE-1 active pharmaceutical ingredient (API) or MINASTRIN 24 FE-1 finished formulations upon request. The MINASTRIN 24 FE-1 suppliers may include MINASTRIN 24 FE-1 API manufacturers, exporters, distributors and traders.
click here to find a list of MINASTRIN 24 FE-1 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing MINASTRIN 24 FE-1 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for MINASTRIN 24 FE-1 API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture MINASTRIN 24 FE-1 as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain MINASTRIN 24 FE-1 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MINASTRIN 24 FE-1 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of MINASTRIN 24 FE-1 suppliers with NDC on PharmaCompass.
We have 4 companies offering MINASTRIN 24 FE-1
Get in contact with the supplier of your choice:
