Package 72162-1535-1

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1535-1
Digits Only 7216215351
Product NDC 72162-1535
Product ID 72162-1535_87e2972a-b207-4248-a0f7-a2719961751f
Description

100 TABLET in 1 BOTTLE (72162-1535-1)

Marketing

Marketing Status
Marketed Since 2024-02-02
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Hydralazine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "87e2972a-b207-4248-a0f7-a2719961751f", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905199"], "spl_set_id": ["4d1594dc-376b-44bd-8c0e-5de731dfb7f9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1535-0)", "package_ndc": "72162-1535-0", "marketing_start_date": "20240202"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1535-1)", "package_ndc": "72162-1535-1", "marketing_start_date": "20240202"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "72162-1535_87e2972a-b207-4248-a0f7-a2719961751f", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "72162-1535", "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": "10 mg/1"}], "application_number": "ANDA205236", "marketing_category": "ANDA", "marketing_start_date": "20170526", "listing_expiration_date": "20261231"}