Package 71335-1589-1

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-1589-1
Digits Only 7133515891
Product NDC 71335-1589
Description

30 TABLET in 1 BOTTLE (71335-1589-1)

Marketing

Marketing Status
Marketed Since 2014-09-12
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": "15abfa42-46a4-441c-aca2-25377e0719db", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905222", "905225"], "spl_set_id": ["d2d98842-ff32-4a61-94e0-60e06919948f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1589-1)", "package_ndc": "71335-1589-1", "marketing_start_date": "20140912"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1589-2)", "package_ndc": "71335-1589-2", "marketing_start_date": "20140912"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1589-3)", "package_ndc": "71335-1589-3", "marketing_start_date": "20140912"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "71335-1589_15abfa42-46a4-441c-aca2-25377e0719db", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "71335-1589", "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"}