Package 63629-5696-2
Brand: hydralazine hydrochloride
Generic: hydralazine hydrochloridePackage Facts
Identity
Package NDC
63629-5696-2
Digits Only
6362956962
Product NDC
63629-5696
Description
60 TABLET, FILM COATED in 1 BOTTLE (63629-5696-2)
Marketing
Marketing Status
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": "989ad2d9-0548-4cf8-8fdf-99e18bbb24e6", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905225"], "spl_set_id": ["db138daf-2d2d-4730-a621-a1bd209d5b9f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-5696-1)", "package_ndc": "63629-5696-1", "marketing_start_date": "20170629"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63629-5696-2)", "package_ndc": "63629-5696-2", "marketing_start_date": "20160624"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63629-5696-3)", "package_ndc": "63629-5696-3", "marketing_start_date": "20150715"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (63629-5696-4)", "package_ndc": "63629-5696-4", "marketing_start_date": "20240402"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "63629-5696_989ad2d9-0548-4cf8-8fdf-99e18bbb24e6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "63629-5696", "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": "ANDA086242", "marketing_category": "ANDA", "marketing_start_date": "20070406", "listing_expiration_date": "20261231"}