Package 71335-9722-2

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-9722-2
Digits Only 7133597222
Product NDC 71335-9722
Description

60 TABLET in 1 BOTTLE (71335-9722-2)

Marketing

Marketing Status
Marketed Since 2023-05-30
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": "58bc1add-d89b-4604-811f-3bc0534658aa", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905222"], "spl_set_id": ["d4509f69-e60e-4440-957b-5c2714480335"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9722-1)", "package_ndc": "71335-9722-1", "marketing_start_date": "20230530"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-9722-2)", "package_ndc": "71335-9722-2", "marketing_start_date": "20230530"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-9722-3)", "package_ndc": "71335-9722-3", "marketing_start_date": "20230530"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "71335-9722_58bc1add-d89b-4604-811f-3bc0534658aa", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "71335-9722", "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": "ANDA205236", "marketing_category": "ANDA", "marketing_start_date": "20170526", "listing_expiration_date": "20261231"}