hydralazine hydrochloride

Generic: hydralazine hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydralazine hydrochloride
Generic Name hydralazine hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydralazine hydrochloride 25 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2352
Product ID 71335-2352_c500c938-29f9-44a4-ade1-6915016fc952
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205236
Listing Expiration 2026-12-31
Marketing Start 2017-05-26

Pharmacologic Class

Classes
arteriolar vasodilation [pe] arteriolar vasodilator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352352
Hyphenated Format 71335-2352

Supplemental Identifiers

RxCUI
905225
UNII
FD171B778Y

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name hydralazine hydrochloride (source: ndc)
Generic Name hydralazine hydrochloride (source: ndc)
Application Number ANDA205236 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-2352-1)
  • 60 TABLET in 1 BOTTLE (71335-2352-2)
  • 90 TABLET in 1 BOTTLE (71335-2352-3)
  • 10 TABLET in 1 BOTTLE (71335-2352-4)
  • 100 TABLET in 1 BOTTLE (71335-2352-5)
source: ndc

Packages (5)

71335-2352-1 30 TABLET in 1 BOTTLE (71335-2352-1) 71335-2352-2 60 TABLET in 1 BOTTLE (71335-2352-2) 71335-2352-3 90 TABLET in 1 BOTTLE (71335-2352-3) 71335-2352-4 10 TABLET in 1 BOTTLE (71335-2352-4) 71335-2352-5 100 TABLET in 1 BOTTLE (71335-2352-5)

Ingredients (1)

hydralazine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Hydralazine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c500c938-29f9-44a4-ade1-6915016fc952", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905225"], "spl_set_id": ["ff2c4d1e-33ee-40d7-955b-d736f0559f39"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2352-1)", "package_ndc": "71335-2352-1", "marketing_start_date": "20240221"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2352-2)", "package_ndc": "71335-2352-2", "marketing_start_date": "20240221"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2352-3)", "package_ndc": "71335-2352-3", "marketing_start_date": "20240221"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-2352-4)", "package_ndc": "71335-2352-4", "marketing_start_date": "20240221"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2352-5)", "package_ndc": "71335-2352-5", "marketing_start_date": "20240221"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "71335-2352_c500c938-29f9-44a4-ade1-6915016fc952", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "71335-2352", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA205236", "marketing_category": "ANDA", "marketing_start_date": "20170526", "listing_expiration_date": "20261231"}