Package 68071-3408-1

Brand: enalapril maleate

Generic: enalapril maleate
NDC Package

Package Facts

Identity

Package NDC 68071-3408-1
Digits Only 6807134081
Product NDC 68071-3408
Description

100 TABLET in 1 BOTTLE (68071-3408-1)

Marketing

Marketing Status
Marketed Since 2023-06-15
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": "2ac0f9b5-bf8e-9c61-e063-6294a90abce6", "openfda": {"upc": ["0368071340815"], "unii": ["9O25354EPJ"], "rxcui": ["858810"], "spl_set_id": ["fe2dfa84-0276-6603-e053-6394a90af8ee"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-3408-1)", "package_ndc": "68071-3408-1", "marketing_start_date": "20230615"}], "brand_name": "Enalapril Maleate", "product_id": "68071-3408_2ac0f9b5-bf8e-9c61-e063-6294a90abce6", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68071-3408", "generic_name": "Enalapril Maleate", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "20 mg/1"}], "application_number": "ANDA213273", "marketing_category": "ANDA", "marketing_start_date": "20220424", "listing_expiration_date": "20261231"}