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 1Aarti Pharmalabs Limited
03 1Farmhispania, S.A.
04 1AX Pharmaceutical Corp
05 1Aurobindo Pharma Limited
06 1Darmerica, LLC
07 1Novartis Pharma Schweizerhalle AG
08 1Professional Compounding Centers of America dba PCCA
09 2ScinoPharm Taiwan Ltd.
10 1W. R. GRACE & CO.-CONN.
11 1Wisdom Pharmaceutical Co.,Ltd
12 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD.
01 1BENAZEPRIL HYDROCHLORIDE
02 11Benazepril Hydrochloride
03 1benazepril hydrochloride
01 1Canada
02 2China
03 3India
04 1Spain
05 1Switzerland
06 2Taiwan
07 2U.S.A
08 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 : 58159-086
Start Marketing Date : 2021-06-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
NDC Package Code : 15308-0900
Start Marketing Date : 1992-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
NDC Package Code : 17404-0016
Start Marketing Date : 2003-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22568-1136
Start Marketing Date : 2021-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 44139-0026
Start Marketing Date : 1995-03-03
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0036
Start Marketing Date : 2019-12-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 65129-2021
Start Marketing Date : 2002-12-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65129-2021
Start Marketing Date : 2002-12-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 13612-0002
Start Marketing Date : 2019-03-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64220-145
Start Marketing Date : 2005-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Benazepril Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benazepril Hydrochloride, including repackagers and relabelers. The FDA regulates Benazepril Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benazepril 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 Benazepril Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Benazepril Hydrochloride supplier is an individual or a company that provides Benazepril Hydrochloride active pharmaceutical ingredient (API) or Benazepril Hydrochloride finished formulations upon request. The Benazepril Hydrochloride suppliers may include Benazepril Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Benazepril 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 Benazepril Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Benazepril 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 Benazepril 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 Benazepril Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Benazepril Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Benazepril Hydrochloride suppliers with NDC on PharmaCompass.
We have 12 companies offering Benazepril Hydrochloride
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
