Package 63629-8497-1

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-8497-1
Digits Only 6362984971
Product NDC 63629-8497
Product ID 63629-8497_0a3f1261-d3e3-4f67-9a28-01edbf99635e
Description

1000 TABLET in 1 BOTTLE (63629-8497-1)

Marketing

Marketing Status
Marketed Since 2021-05-18
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": "0a3f1261-d3e3-4f67-9a28-01edbf99635e", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905395"], "spl_set_id": ["18dd864f-1e27-4c98-8f21-eaded77a3ed6"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (63629-8497-1)", "package_ndc": "63629-8497-1", "marketing_start_date": "20210518"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "63629-8497_0a3f1261-d3e3-4f67-9a28-01edbf99635e", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "63629-8497", "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": "50 mg/1"}], "application_number": "ANDA205236", "marketing_category": "ANDA", "marketing_start_date": "20170526", "listing_expiration_date": "20261231"}