NDC 67877-292

Hydralazine Hydrochloride

Hydralazine Hydrochloride

Hydralazine Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Ascend Laboratories, Llc. The primary component is Hydralazine Hydrochloride.

Product ID67877-292_26a904df-7070-489e-b0e0-67167a817944
NDC67877-292
Product TypeHuman Prescription Drug
Proprietary NameHydralazine Hydrochloride
Generic NameHydralazine Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2010-05-24
Marketing CategoryANDA / ANDA
Application NumberANDA200737
Labeler NameAscend Laboratories, LLC
Substance NameHYDRALAZINE HYDROCHLORIDE
Active Ingredient Strength25 mg/1
Pharm ClassesArteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 67877-292-01

100 TABLET in 1 BOTTLE (67877-292-01)
Marketing Start Date2010-05-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67877-292-00 [67877029200]

Hydralazine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA200737
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-05-24
Marketing End Date2013-03-04

NDC 67877-292-10 [67877029210]

Hydralazine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA200737
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-05-24

NDC 67877-292-01 [67877029201]

Hydralazine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA200737
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-05-24

NDC 67877-292-05 [67877029205]

Hydralazine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA200737
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-05-24

NDC 67877-292-20 [67877029220]

Hydralazine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA200737
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-05-24
Marketing End Date2013-03-04

NDC 67877-292-50 [67877029250]

Hydralazine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA200737
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-05-24
Marketing End Date2013-03-04

Drug Details

Active Ingredients

IngredientStrength
HYDRALAZINE HYDROCHLORIDE25 mg/1

OpenFDA Data

SPL SET ID:e7bfec3d-5222-4a26-8f99-6c2a28e14aa6
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 905225
  • 905222
  • 905199
  • 905395
  • UPC Code
  • 0367877293011
  • Pharmacological Class

    • Arteriolar Vasodilation [PE]
    • Arteriolar Vasodilator [EPC]
    • Arteriolar Vasodilation [PE]
    • Arteriolar Vasodilator [EPC]

    NDC Crossover Matching brand name "Hydralazine Hydrochloride" or generic name "Hydralazine Hydrochloride"

    NDCBrand NameGeneric Name
    0404-9875HYDRALAZINE HYDROCHLORIDEhydralazine hydrochloride
    0404-9986HYDRALAZINE HYDROCHLORIDEhydralazine hydrochloride
    0517-0901Hydralazine HydrochlorideHydralazine Hydrochloride
    0615-0516Hydralazine HydrochlorideHydralazine Hydrochloride
    0615-0531Hydralazine HydrochlorideHydralazine Hydrochloride
    0615-0532Hydralazine HydrochlorideHydralazine Hydrochloride
    0615-5649Hydralazine HydrochlorideHydralazine Hydrochloride
    0615-7973Hydralazine HydrochlorideHydralazine Hydrochloride
    0641-6231HydrALAZINE hydrochlorideHydrALAZINE hydrochloride
    0904-6440Hydralazine HydrochlorideHydralazine Hydrochloride
    0904-6441Hydralazine HydrochlorideHydralazine Hydrochloride
    0904-6442Hydralazine HydrochlorideHydralazine Hydrochloride
    0904-6443Hydralazine HydrochlorideHydralazine Hydrochloride
    17478-834Hydralazine HydrochlorideHydralazine Hydrochloride
    17478-934Hydralazine HydrochlorideHydralazine Hydrochloride
    21695-679HYDRALAZINE HYDROCHLORIDEHydralazine Hydrochloride
    21695-680HYDRALAZINE HYDROCHLORIDEHydralazine Hydrochloride
    21695-694HYDRALAZINE HYDROCHLORIDEHydralazine Hydrochloride
    21695-695HYDRALAZINE HYDROCHLORIDEHydralazine Hydrochloride
    67877-293Hydralazine HydrochlorideHydralazine Hydrochloride
    67877-292Hydralazine HydrochlorideHydralazine Hydrochloride
    67877-291Hydralazine HydrochlorideHydralazine Hydrochloride
    67877-290Hydralazine HydrochlorideHydralazine Hydrochloride
    68071-2055Hydralazine HydrochlorideHydralazine Hydrochloride
    68071-2012Hydralazine HydrochlorideHydralazine Hydrochloride
    68071-3279Hydralazine HydrochlorideHydralazine Hydrochloride
    68071-1940Hydralazine HydrochlorideHydralazine Hydrochloride
    68071-4490Hydralazine HydrochlorideHydralazine Hydrochloride
    68084-447Hydralazine HydrochlorideHydralazine Hydrochloride
    68462-341Hydralazine HydrochlorideHydralazine Hydrochloride
    68462-342Hydralazine HydrochlorideHydralazine Hydrochloride
    68462-343Hydralazine HydrochlorideHydralazine Hydrochloride
    68462-344Hydralazine HydrochlorideHydralazine Hydrochloride
    68788-6917Hydralazine HydrochlorideHydralazine Hydrochloride
    68788-7330Hydralazine HydrochlorideHydralazine Hydrochloride
    70518-0479Hydralazine HydrochlorideHydralazine Hydrochloride
    70518-0666Hydralazine HydrochlorideHydralazine Hydrochloride
    70518-0637Hydralazine HydrochlorideHydralazine Hydrochloride
    70518-0832Hydralazine HydrochlorideHydralazine Hydrochloride
    70518-1685Hydralazine HydrochlorideHydralazine Hydrochloride
    70518-1868Hydralazine HydrochlorideHydralazine Hydrochloride
    70518-1403HydrALAZINE HydrochlorideHydrALAZINE Hydrochloride
    71205-091Hydralazine HydrochlorideHydralazine Hydrochloride
    71209-018HYDRALAZINE HYDROCHLORIDEHYDRALAZINE HYDROCHLORIDE
    71209-017HYDRALAZINE HYDROCHLORIDEHYDRALAZINE HYDROCHLORIDE
    71205-072HydrALAZINE HydrochlorideHydrALAZINE Hydrochloride
    71209-016HYDRALAZINE HYDROCHLORIDEHYDRALAZINE HYDROCHLORIDE
    71335-0983Hydralazine HydrochlorideHydralazine Hydrochloride
    71335-0594Hydralazine HydrochlorideHydralazine Hydrochloride
    71335-0202Hydralazine HydrochlorideHydralazine Hydrochloride

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