Package 50090-5993-0

Brand: alogliptin and metformin hydrochloride

Generic: alogliptin and metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-5993-0
Digits Only 5009059930
Product NDC 50090-5993
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-5993-0)

Marketing

Marketing Status
Marketed Since 2022-06-10
Brand alogliptin and metformin hydrochloride
Generic alogliptin and metformin hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "58968f11-76a2-4e8d-8414-dc636614dedb", "openfda": {"unii": ["EEN99869SC", "786Z46389E"], "rxcui": ["1368385"], "spl_set_id": ["9112d6b9-4771-4194-886d-7db887470bcc"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-5993-0)", "package_ndc": "50090-5993-0", "marketing_start_date": "20220610"}], "brand_name": "alogliptin and metformin hydrochloride", "product_id": "50090-5993_58968f11-76a2-4e8d-8414-dc636614dedb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]", "Dipeptidyl Peptidase 4 Inhibitor [EPC]", "Dipeptidyl Peptidase 4 Inhibitors [MoA]"], "product_ndc": "50090-5993", "generic_name": "alogliptin and metformin hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "alogliptin and metformin hydrochloride", "active_ingredients": [{"name": "ALOGLIPTIN BENZOATE", "strength": "12.5 mg/1"}, {"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "NDA203414", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20160408", "listing_expiration_date": "20261231"}