Package 72789-318-90
Brand: enalapril maleate
Generic: enalapril maleatePackage Facts
Identity
Package NDC
72789-318-90
Digits Only
7278931890
Product NDC
72789-318
Description
90 TABLET in 1 BOTTLE, PLASTIC (72789-318-90)
Marketing
Marketing Status
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": "2e70221c-7705-77b8-e063-6394a90a32a6", "openfda": {"upc": ["0372789318905"], "unii": ["9O25354EPJ"], "rxcui": ["858810"], "spl_set_id": ["cbaaa849-0f9d-4294-b122-090ff17fdcc7"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-318-90)", "package_ndc": "72789-318-90", "marketing_start_date": "20230404"}], "brand_name": "Enalapril Maleate", "product_id": "72789-318_2e70221c-7705-77b8-e063-6394a90a32a6", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "72789-318", "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": "20 mg/1"}], "application_number": "ANDA213273", "marketing_category": "ANDA", "marketing_start_date": "20220424", "listing_expiration_date": "20261231"}