Honour is a leading global CDMO and specialty chemicals manufacturer with seven world-class sites delivering quality-driven solutions.
01 1Honour Lab Limited
02 1Alivus Life Sciences Limited
03 1Apothecon Pharmaceuticals Pvt Ltd
04 1Aurobindo Pharma Limited
05 1Cadila Pharmaceuticals Limited
06 1Chemeca Drugs Private Limited
07 1HETERO LABS LIMITED
08 1Hetero Labs Limited
09 1SOLARA ACTIVE PHARMA SCIENCES LIMITED
10 1Spectrum Laboratory Products, Inc.
11 2Sumitomo Chemical Company, Limited
12 1Wanbury Limited
01 1HYDRALAZINE HYDROCHLORIDE
02 12Hydralazine Hydrochloride
01 10India
02 2Japan
03 1U.S.A
Honour is a leading global CDMO and specialty chemicals manufacturer with seven world-class sites delivering quality-driven solutions.
NDC Package Code : 69037-0047
Start Marketing Date : 1982-01-01
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-957
Start Marketing Date : 2021-02-24
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59651-148
Start Marketing Date : 2024-01-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65691-0088
Start Marketing Date : 2020-07-03
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68554-0148
Start Marketing Date : 1953-01-15
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68554-0023
Start Marketing Date : 1982-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-3544
Start Marketing Date : 2001-02-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68259-1307
Start Marketing Date : 2009-06-18
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68259-1313
Start Marketing Date : 2014-02-27
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62350-0080
Start Marketing Date : 2018-12-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Hydralazine 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 Hydralazine Hydrochloride manufacturer or Hydralazine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydralazine Hydrochloride manufacturer or Hydralazine Hydrochloride supplier.
A Hydralazine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydralazine Hydrochloride, including repackagers and relabelers. The FDA regulates Hydralazine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydralazine 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 Hydralazine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Hydralazine Hydrochloride supplier is an individual or a company that provides Hydralazine Hydrochloride active pharmaceutical ingredient (API) or Hydralazine Hydrochloride finished formulations upon request. The Hydralazine Hydrochloride suppliers may include Hydralazine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Hydralazine Hydrochloride 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 Hydralazine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Hydralazine 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 Hydralazine 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 Hydralazine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Hydralazine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Hydralazine Hydrochloride suppliers with NDC on PharmaCompass.
We have 11 companies offering Hydralazine Hydrochloride
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