hydralazine hydrochloride

Generic: hydralazine hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

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

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2551
Product ID 70518-2551_4a67249e-ac1c-3ea4-e063-6394a90a3fc5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040901
Listing Expiration 2027-12-31
Marketing Start 2020-01-22

Pharmacologic Class

Classes
arteriolar vasodilation [pe] arteriolar vasodilator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182551
Hyphenated Format 70518-2551

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 ANDA040901 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-2551-0)
  • 30 TABLET in 1 BLISTER PACK (70518-2551-1)
  • 180 TABLET in 1 BOTTLE, PLASTIC (70518-2551-2)
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-2551-3)
source: ndc

Packages (4)

70518-2551-0 30 TABLET in 1 BLISTER PACK (70518-2551-0) 70518-2551-1 30 TABLET in 1 BLISTER PACK (70518-2551-1) 70518-2551-2 180 TABLET in 1 BOTTLE, PLASTIC (70518-2551-2) 70518-2551-3 90 TABLET in 1 BOTTLE, PLASTIC (70518-2551-3)

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": "4a67249e-ac1c-3ea4-e063-6394a90a3fc5", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905225"], "spl_set_id": ["89afc8ef-27c4-489a-81de-3f8f65f6bbb8"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2551-0)", "package_ndc": "70518-2551-0", "marketing_start_date": "20200122"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2551-1)", "package_ndc": "70518-2551-1", "marketing_start_date": "20250731"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (70518-2551-2)", "package_ndc": "70518-2551-2", "marketing_start_date": "20250904"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-2551-3)", "package_ndc": "70518-2551-3", "marketing_start_date": "20250904"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "70518-2551_4a67249e-ac1c-3ea4-e063-6394a90a3fc5", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "70518-2551", "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": "ANDA040901", "marketing_category": "ANDA", "marketing_start_date": "20200122", "listing_expiration_date": "20271231"}