Hydralazine Hydrochloride

Generic: Hydralazine Hydrochloride

Labeler: REMEDYREPACK INC.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Hydralazine Hydrochloride
Generic Name Hydralazine Hydrochloride
Labeler REMEDYREPACK INC.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

HYDRALAZINE HYDROCHLORIDE 25 mg/1

Identifiers & Regulatory

Product NDC 70518-4064
Product ID 70518-4064_3bdfd6d4-b5a5-37ca-e063-6394a90a7995
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040858
Listing Expiration 2026-12-31
Marketing Start 2024-05-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184064
Hyphenated Format 70518-4064

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 ANDA040858 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-4064-1)
  • 180 TABLET in 1 BOTTLE, PLASTIC (70518-4064-2)
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-4064-3)
source: ndc

Packages (3)

70518-4064-1 30 TABLET in 1 BLISTER PACK (70518-4064-1) 70518-4064-2 180 TABLET in 1 BOTTLE, PLASTIC (70518-4064-2) 70518-4064-3 90 TABLET in 1 BOTTLE, PLASTIC (70518-4064-3)

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": "3bdfd6d4-b5a5-37ca-e063-6394a90a7995", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905225"], "spl_set_id": ["6c40d818-77a9-492c-b9b6-d8a0fe8d6736"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4064-1)", "package_ndc": "70518-4064-1", "marketing_start_date": "20241220"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (70518-4064-2)", "package_ndc": "70518-4064-2", "marketing_start_date": "20250528"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4064-3)", "package_ndc": "70518-4064-3", "marketing_start_date": "20250701"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "70518-4064_3bdfd6d4-b5a5-37ca-e063-6394a90a7995", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "70518-4064", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040858", "marketing_category": "ANDA", "marketing_start_date": "20240504", "listing_expiration_date": "20261231"}