Package 50090-6684-0

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6684-0
Digits Only 5009066840
Product NDC 50090-6684
Description

90 TABLET in 1 BOTTLE (50090-6684-0)

Marketing

Marketing Status
Marketed Since 2023-09-14
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": "837ac56f-c6ba-49ef-bd34-269b3022b14b", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905395"], "spl_set_id": ["7253aaa0-e272-499f-9bfa-304e9556a8fb"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6684-0)", "package_ndc": "50090-6684-0", "marketing_start_date": "20230914"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "50090-6684_837ac56f-c6ba-49ef-bd34-269b3022b14b", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "50090-6684", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040901", "marketing_category": "ANDA", "marketing_start_date": "20100101", "listing_expiration_date": "20261231"}