Package 63629-8757-1

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-8757-1
Digits Only 6362987571
Product NDC 63629-8757
Product ID 63629-8757_3335c836-5e3d-4b72-b9d1-b3365cbe28b6
Description

1000 TABLET in 1 BOTTLE (63629-8757-1)

Marketing

Marketing Status
Marketed Since 2021-08-20
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": "3335c836-5e3d-4b72-b9d1-b3365cbe28b6", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905225"], "spl_set_id": ["10f3e76e-9bba-4151-89fb-90d823a0a68c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (63629-8757-1)", "package_ndc": "63629-8757-1", "marketing_start_date": "20210820"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "63629-8757_3335c836-5e3d-4b72-b9d1-b3365cbe28b6", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "63629-8757", "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"}