Package 70518-3572-1

Brand: enalapril maleate

Generic: enalapril maleate
NDC Package

Package Facts

Identity

Package NDC 70518-3572-1
Digits Only 7051835721
Product NDC 70518-3572
Description

30 TABLET in 1 BLISTER PACK (70518-3572-1)

Marketing

Marketing Status
Marketed Since 2025-03-03
Brand enalapril maleate
Generic enalapril maleate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4611792f-0f1c-a841-e063-6294a90a2646", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858813"], "spl_set_id": ["1b464099-491d-473b-836e-9d86b2b1eeec"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3572-1)", "package_ndc": "70518-3572-1", "marketing_start_date": "20250303"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3572-2)", "package_ndc": "70518-3572-2", "marketing_start_date": "20250528"}], "brand_name": "Enalapril Maleate", "product_id": "70518-3572_4611792f-0f1c-a841-e063-6294a90a2646", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "70518-3572", "generic_name": "Enalapril Maleate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA213273", "marketing_category": "ANDA", "marketing_start_date": "20221107", "listing_expiration_date": "20261231"}