Package 70518-3852-0

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3852-0
Digits Only 7051838520
Product NDC 70518-3852
Product ID 70518-3852_3f8c1a73-dd59-1bdc-e063-6294a90a54fc
Description

30 TABLET in 1 BLISTER PACK (70518-3852-0)

Marketing

Marketing Status
Marketed Since 2023-09-03
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Hydralazine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f8c1a73-dd59-1bdc-e063-6294a90a54fc", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905225"], "spl_set_id": ["0d65e146-83e5-427f-ac06-04c0d8e72cea"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3852-0)", "package_ndc": "70518-3852-0", "marketing_start_date": "20230903"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "70518-3852_3f8c1a73-dd59-1bdc-e063-6294a90a54fc", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "70518-3852", "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": "ANDA205236", "marketing_category": "ANDA", "marketing_start_date": "20230903", "listing_expiration_date": "20261231"}