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01 1Farmabios S.p.A.
02 1DARMERICA, LLC
03 1Pharmacia and Upjohn Company LLC
04 1Professional Compounding Centers of America dba PCCA
05 1Sicor de Mexico S.A. de C.V
06 1Zhejiang Xianju Pharmaceutical Co., Ltd.
01 2MEGESTROL ACETATE
02 3Megestrol Acetate
03 1megestrol acetate
01 1China
02 1Germany
03 1Mexico
04 2U.S.A
05 1United Kingdom
NDC Package Code : 46439-8722
Start Marketing Date : 1998-07-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-116
Start Marketing Date : 2022-10-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-1670
Start Marketing Date : 2013-06-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0009-5030
Start Marketing Date : 2014-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63592-0109
Start Marketing Date : 2018-10-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60722-1009
Start Marketing Date : 2023-06-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Megestrol Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Megestrol Acetate, including repackagers and relabelers. The FDA regulates Megestrol Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Megestrol 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 Megestrol Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Megestrol Acetate supplier is an individual or a company that provides Megestrol Acetate active pharmaceutical ingredient (API) or Megestrol Acetate finished formulations upon request. The Megestrol Acetate suppliers may include Megestrol Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Megestrol Acetate 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 Megestrol Acetate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Megestrol Acetate 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 Megestrol Acetate 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 Megestrol Acetate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Megestrol Acetate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Megestrol Acetate suppliers with NDC on PharmaCompass.
We have 6 companies offering Megestrol Acetate
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