Package 43353-124-05

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43353-124-05
Digits Only 4335312405
Product NDC 43353-124
Description

4200 TABLET in 1 BOTTLE (43353-124-05)

Marketing

Marketing Status
Marketed Since 2015-12-02
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": "66435209-390b-4344-9b5b-47c9c2d92e2f", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905222"], "spl_set_id": ["d9892176-d4a6-4edb-92b9-5f56243f3d22"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "4200 TABLET in 1 BOTTLE (43353-124-05)", "package_ndc": "43353-124-05", "marketing_start_date": "20151202"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "43353-124_66435209-390b-4344-9b5b-47c9c2d92e2f", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "43353-124", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA089098", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}