Package 72162-1521-0

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1521-0
Digits Only 7216215210
Product NDC 72162-1521
Product ID 72162-1521_2b4aae2f-2c3f-4ff8-9a1d-4c51c9b7f19d
Description

1000 TABLET in 1 BOTTLE (72162-1521-0)

Marketing

Marketing Status
Marketed Since 2024-12-24
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b4aae2f-2c3f-4ff8-9a1d-4c51c9b7f19d", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905225"], "spl_set_id": ["7ae650f7-a481-4637-a9a2-9bda43a5a288"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1521-0)", "package_ndc": "72162-1521-0", "marketing_start_date": "20241224"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "72162-1521_2b4aae2f-2c3f-4ff8-9a1d-4c51c9b7f19d", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "72162-1521", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA088467", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}