Package 70518-4022-0

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4022-0
Digits Only 7051840220
Product NDC 70518-4022
Product ID 70518-4022_3f908b4b-ad9d-0995-e063-6394a90a7cf6
Description

30 TABLET in 1 BLISTER PACK (70518-4022-0)

Marketing

Marketing Status
Marketed Since 2024-02-13
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f908b4b-ad9d-0995-e063-6394a90a7cf6", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905199"], "spl_set_id": ["a70d20d6-23f0-477e-915c-678a86782175"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4022-0)", "package_ndc": "70518-4022-0", "marketing_start_date": "20240213"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4022-1)", "package_ndc": "70518-4022-1", "marketing_start_date": "20250920"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "70518-4022_3f908b4b-ad9d-0995-e063-6394a90a7cf6", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "70518-4022", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA040858", "marketing_category": "ANDA", "marketing_start_date": "20240213", "listing_expiration_date": "20261231"}