Package 71288-205-02

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71288-205-02
Digits Only 7128820502
Product NDC 71288-205
Description

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

Marketing

Marketing Status
Marketed Since 2025-06-02
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

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"}