Package 50090-5574-0

Brand: alogliptin

Generic: alogliptin
NDC Package

Package Facts

Identity

Package NDC 50090-5574-0
Digits Only 5009055740
Product NDC 50090-5574
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-5574-0)

Marketing

Marketing Status
Marketed Since 2021-07-02
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": "b2747bb4-79a6-4e24-aa7c-79fe610523e1", "openfda": {"unii": ["EEN99869SC"], "rxcui": ["1368006"], "spl_set_id": ["38d30e4f-4212-4f7a-96b5-74b277b56cba"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-5574-0)", "package_ndc": "50090-5574-0", "marketing_start_date": "20210702"}], "brand_name": "Alogliptin", "product_id": "50090-5574_b2747bb4-79a6-4e24-aa7c-79fe610523e1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dipeptidyl Peptidase 4 Inhibitor [EPC]", "Dipeptidyl Peptidase 4 Inhibitors [MoA]"], "product_ndc": "50090-5574", "generic_name": "Alogliptin", "labeler_name": "A-S Medication Solutions", "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"}