With Fermion, start the journey of your innovative API.
01 1Fermion Oy
02 1Excella GmbH & Co. KG
03 1LETCO MEDICAL, LLC
04 1Maithri Laboratories Private Limited
05 1Medilux Laboratories Private Limited
06 1Professional Compounding Centers of America
07 1SOLARA ACTIVE PHARMA SCIENCES LIMITED
08 1Spectrum Laboratory Products, Inc.
09 1Unichem Laboratories Limited, India
10 1Zydus Lifesciences Limited
01 2BUSPIRONE HYDROCHLORIDE
02 1Buspirone HCl
03 1Buspirone Hcl
04 4Buspirone Hydrochloride
05 1Buspirone hydrochloride
06 1buspirone hydrochloride
01 1Finland
02 5India
03 1Luxembourg
04 2U.S.A
05 1United Kingdom
With Fermion, start the journey of your innovative API.
NDC Package Code : 12780-2940
Start Marketing Date : 1994-10-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46014-1068
Start Marketing Date : 2012-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-2845
Start Marketing Date : 2010-11-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 50218-013
Start Marketing Date : 2024-04-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 71666-013
Start Marketing Date : 2023-03-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0169
Start Marketing Date : 2018-12-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 72643-036
Start Marketing Date : 2023-07-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-1310
Start Marketing Date : 2006-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53747-040
Start Marketing Date : 2015-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65841-136
Start Marketing Date : 2024-11-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Buspirone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Buspirone Hydrochloride, including repackagers and relabelers. The FDA regulates Buspirone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Buspirone Hydrochloride 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 Buspirone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Buspirone Hydrochloride supplier is an individual or a company that provides Buspirone Hydrochloride active pharmaceutical ingredient (API) or Buspirone Hydrochloride finished formulations upon request. The Buspirone Hydrochloride suppliers may include Buspirone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Buspirone Hydrochloride 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 Buspirone Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Buspirone Hydrochloride 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 Buspirone Hydrochloride 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 Buspirone Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Buspirone Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Buspirone Hydrochloride suppliers with NDC on PharmaCompass.
We have 10 companies offering Buspirone Hydrochloride
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