Package 63629-4946-1

Brand: alogliptin

Generic: alogliptin
NDC Package

Package Facts

Identity

Package NDC 63629-4946-1
Digits Only 6362949461
Product NDC 63629-4946
Description

30 TABLET, FILM COATED in 1 BOTTLE (63629-4946-1)

Marketing

Marketing Status
Marketed Since 2025-01-28
Brand alogliptin
Generic alogliptin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "92219b66-aacf-4ddc-9320-9ea8f620ab8c", "openfda": {"unii": ["EEN99869SC"], "rxcui": ["1368006"], "spl_set_id": ["f2ad6d21-8060-42c7-8b3f-ad80085dc022"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-4946-1)", "package_ndc": "63629-4946-1", "marketing_start_date": "20250128"}], "brand_name": "Alogliptin", "product_id": "63629-4946_92219b66-aacf-4ddc-9320-9ea8f620ab8c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dipeptidyl Peptidase 4 Inhibitor [EPC]", "Dipeptidyl Peptidase 4 Inhibitors [MoA]"], "product_ndc": "63629-4946", "generic_name": "Alogliptin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alogliptin", "active_ingredients": [{"name": "ALOGLIPTIN BENZOATE", "strength": "25 mg/1"}], "application_number": "NDA022271", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20160408", "listing_expiration_date": "20261231"}