Package 71872-7274-1

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71872-7274-1
Digits Only 7187272741
Product NDC 71872-7274
Description

1 VIAL, SINGLE-DOSE in 1 BAG (71872-7274-1) / 20 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2021-12-09
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": "facb9282-cc50-7e82-e053-6294a90af0aa", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["d89d981d-64cf-7321-e053-2995a90aab4a"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (71872-7274-1)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71872-7274-1", "marketing_start_date": "20211209"}], "brand_name": "HydrALAZINE hydrochloride", "product_id": "71872-7274_facb9282-cc50-7e82-e053-6294a90af0aa", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "71872-7274", "generic_name": "HydrALAZINE hydrochloride", "labeler_name": "Medical Purchasing Solutions, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HydrALAZINE hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA213667", "marketing_category": "ANDA", "marketing_start_date": "20201218", "listing_expiration_date": "20261231"}