Package 71610-661-18
Brand: alogliptin
Generic: alogliptinPackage Facts
Identity
Package NDC
71610-661-18
Digits Only
7161066118
Product NDC
71610-661
Description
3000 TABLET, FILM COATED in 1 BOTTLE (71610-661-18)
Marketing
Marketing Status
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": "7ecf7f4e-e65c-4dde-9db9-20a170a427c9", "openfda": {"unii": ["EEN99869SC"], "rxcui": ["1368034"], "spl_set_id": ["a05d6d17-79f9-4788-a4d5-467bca1a2d91"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "9000 TABLET, FILM COATED in 1 BOTTLE (71610-661-09)", "package_ndc": "71610-661-09", "marketing_start_date": "20220908"}, {"sample": false, "description": "3000 TABLET, FILM COATED in 1 BOTTLE (71610-661-18)", "package_ndc": "71610-661-18", "marketing_start_date": "20221017"}], "brand_name": "Alogliptin", "product_id": "71610-661_7ecf7f4e-e65c-4dde-9db9-20a170a427c9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dipeptidyl Peptidase 4 Inhibitor [EPC]", "Dipeptidyl Peptidase 4 Inhibitors [MoA]"], "product_ndc": "71610-661", "generic_name": "Alogliptin", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alogliptin", "active_ingredients": [{"name": "ALOGLIPTIN BENZOATE", "strength": "12.5 mg/1"}], "application_number": "NDA022271", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20160408", "listing_expiration_date": "20261231"}