Package 63629-5424-3

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-5424-3
Digits Only 6362954243
Product NDC 63629-5424
Description

90 TABLET in 1 BOTTLE (63629-5424-3)

Marketing

Marketing Status
Marketed Since 2017-11-20
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1bccffd8-62f7-4dc3-8bb9-c47287c718a3", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905222"], "spl_set_id": ["d79eb016-30c0-4d3f-b854-ada5a43fe5f7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-5424-1)", "package_ndc": "63629-5424-1", "marketing_start_date": "20140910"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63629-5424-2)", "package_ndc": "63629-5424-2", "marketing_start_date": "20151210"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63629-5424-3)", "package_ndc": "63629-5424-3", "marketing_start_date": "20171120"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-5424-4)", "package_ndc": "63629-5424-4", "marketing_start_date": "20240402"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "63629-5424_1bccffd8-62f7-4dc3-8bb9-c47287c718a3", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "63629-5424", "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": "100 mg/1"}], "application_number": "ANDA040901", "marketing_category": "ANDA", "marketing_start_date": "20100101", "listing_expiration_date": "20261231"}