Package 70518-4256-0

Brand: enalapril maleate

Generic: enalapril maleate
NDC Package

Package Facts

Identity

Package NDC 70518-4256-0
Digits Only 7051842560
Product NDC 70518-4256
Description

30 TABLET in 1 BLISTER PACK (70518-4256-0)

Marketing

Marketing Status
Marketed Since 2025-01-15
Brand enalapril maleate
Generic enalapril maleate
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4008b194-eaf3-53aa-e063-6394a90ac6ce", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858817"], "spl_set_id": ["3fbc6cce-7ad5-49d5-9705-5f66ef92d544"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4256-0)", "package_ndc": "70518-4256-0", "marketing_start_date": "20250115"}], "brand_name": "Enalapril Maleate", "product_id": "70518-4256_4008b194-eaf3-53aa-e063-6394a90ac6ce", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "70518-4256", "generic_name": "Enalapril Maleate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA075657", "marketing_category": "ANDA", "marketing_start_date": "20250115", "listing_expiration_date": "20261231"}