Package 72789-329-90

Brand: enalapril maleate

Generic: enalapril maleate
NDC Package

Package Facts

Identity

Package NDC 72789-329-90
Digits Only 7278932990
Product NDC 72789-329
Description

90 TABLET in 1 BOTTLE, PLASTIC (72789-329-90)

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": "2e80ce80-c964-8dbb-e063-6394a90ae43b", "openfda": {"upc": ["0372789329901"], "unii": ["9O25354EPJ"], "rxcui": ["858817"], "spl_set_id": ["fe303f6a-4a9f-259e-e053-6394a90af16b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-329-90)", "package_ndc": "72789-329-90", "marketing_start_date": "20230615"}], "brand_name": "Enalapril Maleate", "product_id": "72789-329_2e80ce80-c964-8dbb-e063-6394a90ae43b", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "72789-329", "generic_name": "Enalapril Maleate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA213273", "marketing_category": "ANDA", "marketing_start_date": "20220424", "listing_expiration_date": "20261231"}