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NDC 64764-250, alogliptin, tablet, film coated, from Takeda Pharmaceuticals America, Inc..

Product NDC
64764-250
Status
Listed
Labeler
Takeda Pharmaceuticals America, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA022271
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/64764-250 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALOGLIPTIN BENZOATE25 mg/1

Pharmacologic classes

Dipeptidyl Peptidase 4 Inhibitor [EPC]; Dipeptidyl Peptidase 4 Inhibitors [MoA]

Package NDCNDC-11Package
64764-250-02647640250024 CARTON in 1 TRAY (64764-250-02) / 1 BLISTER PACK in 1 CARTON / 7 TABLET, FILM COATED in 1 BLISTER PACK
64764-250-306476402503030 TABLET, FILM COATED in 1 BOTTLE (64764-250-30)
64764-250-5064764025050500 TABLET, FILM COATED in 1 BOTTLE (64764-250-50)
64764-250-906476402509090 TABLET, FILM COATED in 1 BOTTLE (64764-250-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a3768c7e-aa4c-44d3-bc53-43bb7346c0b0

Use it

Look up 64764-250 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/64764-250 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 64764-250. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.