Package 70518-4007-1
Brand: hydralazine hydrochloride
Generic: hydralazine hydrochloridePackage Facts
Identity
Package NDC
70518-4007-1
Digits Only
7051840071
Product NDC
70518-4007
Description
90 TABLET in 1 BOTTLE, PLASTIC (70518-4007-1)
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": "36485b76-12c0-7058-e063-6294a90a0eb4", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905395"], "spl_set_id": ["d61ffa06-8138-4a1d-9530-095a80d9c9ce"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4007-0)", "package_ndc": "70518-4007-0", "marketing_start_date": "20240201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4007-1)", "package_ndc": "70518-4007-1", "marketing_start_date": "20250529"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "70518-4007_36485b76-12c0-7058-e063-6294a90a0eb4", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "70518-4007", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040858", "marketing_category": "ANDA", "marketing_start_date": "20240201", "listing_expiration_date": "20261231"}