Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1NURAY CHEMICALS PRIVATE LIMITED
02 1Synthokem Labs Private Limited
03 1Granules India Limited
04 1Bioindustria L.I.M. SpA
05 1DARMERICA, LLC
06 1MSN Organics Private Limited
07 1Pfizer Ireland Pharmaceuticals
08 1Professional Compounding Centers of America dba PCCA
09 1n.v. Ajinomoto Omnichem S.A.
01 2PRAZOSIN HYDROCHLORIDE
02 1Prazosin HCl
03 5Prazosin Hydrochloride
04 1prazosin hydrochloride
01 4India
02 1Italy
03 1Japan
04 2U.S.A
05 1United Kingdom
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-043
Start Marketing Date : 2020-03-03
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Synthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
NDC Package Code : 58343-0140
Start Marketing Date : 2022-10-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
NDC Package Code : 62207-974
Start Marketing Date : 2021-04-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50923-0462
Start Marketing Date : 2009-10-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63809-2742
Start Marketing Date : 2003-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-132
Start Marketing Date : 2020-03-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50379-0019
Start Marketing Date : 2016-02-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-5040
Start Marketing Date : 2018-08-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 60715-0011
Start Marketing Date : 2020-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Prazosin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prazosin Hydrochloride, including repackagers and relabelers. The FDA regulates Prazosin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prazosin 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 Prazosin Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prazosin Hydrochloride supplier is an individual or a company that provides Prazosin Hydrochloride active pharmaceutical ingredient (API) or Prazosin Hydrochloride finished formulations upon request. The Prazosin Hydrochloride suppliers may include Prazosin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Prazosin 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 Prazosin Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Prazosin 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 Prazosin 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 Prazosin Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Prazosin Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Prazosin Hydrochloride suppliers with NDC on PharmaCompass.
We have 9 companies offering Prazosin Hydrochloride
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
