Package 50090-7212-0

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7212-0
Digits Only 5009072120
Product NDC 50090-7212
Product ID 50090-7212_411ffc86-b906-49fd-aafd-42d16e6997ea
Description

90 TABLET in 1 BOTTLE (50090-7212-0)

Marketing

Marketing Status
Marketed Since 2024-08-05
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Hydralazine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "411ffc86-b906-49fd-aafd-42d16e6997ea", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905395"], "spl_set_id": ["8ade1ffe-3738-4aa1-b9c7-59f7290600b9"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7212-0)", "package_ndc": "50090-7212-0", "marketing_start_date": "20240805"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "50090-7212_411ffc86-b906-49fd-aafd-42d16e6997ea", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "50090-7212", "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": "ANDA205236", "marketing_category": "ANDA", "marketing_start_date": "20170526", "listing_expiration_date": "20261231"}