Package 70518-4064-2

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4064-2
Digits Only 7051840642
Product NDC 70518-4064
Description

180 TABLET in 1 BOTTLE, PLASTIC (70518-4064-2)

Marketing

Marketing Status
Marketed Since 2025-05-28
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": "4c994e23-d3bb-f74a-e063-6294a90a6f1d", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905225"], "spl_set_id": ["6c40d818-77a9-492c-b9b6-d8a0fe8d6736"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (70518-4064-2)", "package_ndc": "70518-4064-2", "marketing_start_date": "20250528"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4064-3)", "package_ndc": "70518-4064-3", "marketing_start_date": "20250701"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "70518-4064_4c994e23-d3bb-f74a-e063-6294a90a6f1d", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "70518-4064", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040858", "marketing_category": "ANDA", "marketing_start_date": "20240504", "listing_expiration_date": "20271231"}