Package 71209-017-11

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71209-017-11
Digits Only 7120901711
Product NDC 71209-017
Description

1000 TABLET in 1 BOTTLE (71209-017-11)

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": "4cdbf75c-b17f-4c40-bd7c-7b07668e9659", "openfda": {"upc": ["0371209018050"], "unii": ["FD171B778Y"], "rxcui": ["905222", "905225", "905395"], "spl_set_id": ["3a7562a8-2f67-4411-ac4a-ab7924193e82"], "manufacturer_name": ["Cadila Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71209-017-05)", "package_ndc": "71209-017-05", "marketing_start_date": "20151229"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71209-017-11)", "package_ndc": "71209-017-11", "marketing_start_date": "20151229"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "71209-017_4cdbf75c-b17f-4c40-bd7c-7b07668e9659", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "71209-017", "generic_name": "hydralazine hydrochloride", "labeler_name": "Cadila Pharmaceuticals Limited", "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"}