# Nesina

NDC: 64764-250
Generic name: alogliptin
Labeler / Manufacturer: Takeda Pharmaceuticals America, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20130125

FDA application: NDA022271

## Active ingredients

- ALOGLIPTIN BENZOATE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"64764-250"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64764-250
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a3768c7e-aa4c-44d3-bc53-43bb7346c0b0