Package 50090-6684-0
Brand: hydralazine hydrochloride
Generic: hydralazine hydrochloridePackage 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
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"}