hydralazine hydrochloride

Generic: hydralazine hydrochloride

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

Drug Facts

Product Profile

Brand Name hydralazine hydrochloride
Generic Name hydralazine hydrochloride
Labeler meitheal pharmaceuticals inc.
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

hydralazine hydrochloride 20 mg/mL

Manufacturer
Meitheal Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 71288-205
Product ID 71288-205_9c7f84bf-c884-49fd-8f1f-d368f64d63ff
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217501
Listing Expiration 2026-12-31
Marketing Start 2025-06-02

Pharmacologic Class

Classes
arteriolar vasodilation [pe] arteriolar vasodilator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71288205
Hyphenated Format 71288-205

Supplemental Identifiers

RxCUI
966571
UNII
FD171B778Y

Packaging Origin

Original Packager
true

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 ANDA217501 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-205-02) / 1 mL in 1 VIAL, SINGLE-DOSE (71288-205-01)
source: ndc

Packages (1)

71288-205-02 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-205-02) / 1 mL in 1 VIAL, SINGLE-DOSE (71288-205-01)

Ingredients (1)

hydralazine hydrochloride (20 mg/mL)

Linked Drug Pages (1)

HYDRALAZINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "9c7f84bf-c884-49fd-8f1f-d368f64d63ff", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["f3c806a4-b971-421c-bcb9-9979c6d7aaec"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (71288-205-02)  / 1 mL in 1 VIAL, SINGLE-DOSE (71288-205-01)", "package_ndc": "71288-205-02", "marketing_start_date": "20250602"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "71288-205_9c7f84bf-c884-49fd-8f1f-d368f64d63ff", "dosage_form": "INJECTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "71288-205", "generic_name": "HYDRALAZINE HYDROCHLORIDE", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDRALAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA217501", "marketing_category": "ANDA", "marketing_start_date": "20250602", "listing_expiration_date": "20261231"}