Axplora- The partner of choice for complex APIs.
01 1Farmabios S.p.A.
02 1NURAY CHEMICALS PRIVATE LIMITED
03 1Apicore US LLC
04 1Curia Spain S.A.U.
05 1LETCO MEDICAL, LLC
06 1Medisca Inc.
07 1Professional Compounding Centers of America dba PCCA
08 1Sicor S.r.l.
01 3FLUDROCORTISONE ACETATE
02 3Fludrocortisone Acetate
03 1Fludrocortisone Acetate Micron.
04 1Fludrocortisone acetate
01 1Germany
02 2India
03 1Italy
04 3U.S.A
05 1United Kingdom
Axplora- The partner of choice for complex APIs.
NDC Package Code : 46439-8721
Start Marketing Date : 1999-05-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-074
Start Marketing Date : 2020-02-03
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14096-127
Start Marketing Date : 2007-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65089-0015
Start Marketing Date : 2011-07-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 62991-2773
Start Marketing Date : 2009-05-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0129
Start Marketing Date : 2015-08-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-2408
Start Marketing Date : 2013-06-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 53183-0207
Start Marketing Date : 2010-09-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Fludrocortisone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fludrocortisone Acetate, including repackagers and relabelers. The FDA regulates Fludrocortisone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fludrocortisone 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 Fludrocortisone Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fludrocortisone Acetate supplier is an individual or a company that provides Fludrocortisone Acetate active pharmaceutical ingredient (API) or Fludrocortisone Acetate finished formulations upon request. The Fludrocortisone Acetate suppliers may include Fludrocortisone Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Fludrocortisone 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 Fludrocortisone Acetate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fludrocortisone 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 Fludrocortisone 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 Fludrocortisone Acetate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fludrocortisone Acetate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fludrocortisone Acetate suppliers with NDC on PharmaCompass.
We have 8 companies offering Fludrocortisone Acetate
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