Package 70518-4352-0

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4352-0
Digits Only 7051843520
Product NDC 70518-4352
Product ID 70518-4352_37f097fd-43b5-3c7d-e063-6394a90ae2f8
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-4352-0)

Marketing

Marketing Status
Marketed Since 2025-06-03
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": "37f097fd-43b5-3c7d-e063-6394a90ae2f8", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905222"], "spl_set_id": ["51c293c1-70e7-48c7-8af1-a8b74312ed56"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4352-0)", "package_ndc": "70518-4352-0", "marketing_start_date": "20250603"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4352-1)", "package_ndc": "70518-4352-1", "marketing_start_date": "20250619"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "70518-4352_37f097fd-43b5-3c7d-e063-6394a90ae2f8", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "70518-4352", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA040858", "marketing_category": "ANDA", "marketing_start_date": "20250603", "listing_expiration_date": "20261231"}