Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
01 1Aarti Pharmalabs Limited
02 1AX Pharmaceutical Corp
03 1Aurobindo Pharma Limited
04 1Darmerica, LLC
05 1Emcure Pharmaceuticals Limited
06 1Farmhispania, S.A.
07 1Professional Compounding Centers of America dba PCCA
08 2ScinoPharm Taiwan Ltd.
09 1W. R. GRACE & CO.-CONN.
10 1Wisdom Pharmaceutical Co.,Ltd
11 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD.
01 1BENAZEPRIL HYDROCHLORIDE
02 11Benazepril Hydrochloride
01 1Canada
02 2China
03 3India
04 1Spain
05 2Taiwan
06 2U.S.A
07 1United Kingdom
Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
NDC Package Code : 15308-0900
Start Marketing Date : 1992-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-346
Start Marketing Date : 2023-12-25
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-952
Start Marketing Date : 2025-02-05
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17404-0016
Start Marketing Date : 2003-12-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22568-1136
Start Marketing Date : 2021-06-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0036
Start Marketing Date : 2019-12-17
End Marketing Date : 2026-12-31
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 : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65129-2021
Start Marketing Date : 2002-12-30
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 13612-0002
Start Marketing Date : 2019-03-21
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64220-145
Start Marketing Date : 2005-12-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
11
PharmaCompass offers a list of Benazepril Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Benazepril Hydrochloride manufacturer or Benazepril Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benazepril Hydrochloride manufacturer or Benazepril Hydrochloride supplier.
A KB-65121 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KB-65121, including repackagers and relabelers. The FDA regulates KB-65121 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KB-65121 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 KB-65121 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A KB-65121 supplier is an individual or a company that provides KB-65121 active pharmaceutical ingredient (API) or KB-65121 finished formulations upon request. The KB-65121 suppliers may include KB-65121 API manufacturers, exporters, distributors and traders.
click here to find a list of KB-65121 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 KB-65121 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for KB-65121 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 KB-65121 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 KB-65121 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a KB-65121 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of KB-65121 suppliers with NDC on PharmaCompass.
We have 11 companies offering KB-65121
Get in contact with the supplier of your choice:
