Package 72241-005-11

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72241-005-11
Digits Only 7224100511
Product NDC 72241-005
Description

1000 TABLET in 1 BOTTLE (72241-005-11)

Marketing

Marketing Status
Marketed Since 2015-12-29
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": "2be4a232-7aa2-44f8-ba8c-f5b64677c1b7", "openfda": {"upc": ["0372241006111"], "unii": ["FD171B778Y"], "rxcui": ["905222", "905225", "905395"], "spl_set_id": ["a456bc34-0c79-44f4-9119-50028a978f5f"], "manufacturer_name": ["Modavar Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72241-005-05)", "package_ndc": "72241-005-05", "marketing_start_date": "20151229"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72241-005-11)", "package_ndc": "72241-005-11", "marketing_start_date": "20151229"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "72241-005_2be4a232-7aa2-44f8-ba8c-f5b64677c1b7", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "72241-005", "generic_name": "hydralazine hydrochloride", "labeler_name": "Modavar Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDRALAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA203845", "marketing_category": "ANDA", "marketing_start_date": "20151229", "listing_expiration_date": "20261231"}