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NDC 64764-750, vortioxetine, tablet, film coated, from Takeda Pharmaceuticals America, Inc..

Product NDC
64764-750
Status
Listed
Labeler
Takeda Pharmaceuticals America, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA204447
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/64764-750 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VORTIOXETINE HYDROBROMIDE20 mg/1
Package NDCNDC-11Package
64764-750-07647640750071 BOTTLE in 1 CARTON (64764-750-07) / 7 TABLET, FILM COATED in 1 BOTTLE
64764-750-096476407500930 TABLET, FILM COATED in 1 BOTTLE (64764-750-09)
64764-750-306476407503030 TABLET, FILM COATED in 1 BOTTLE (64764-750-30)
64764-750-7764764075077500 TABLET, FILM COATED in 1 BOTTLE (64764-750-77)
64764-750-906476407509090 TABLET, FILM COATED in 1 BOTTLE (64764-750-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1a5b68e2-14d0-419d-9ec6-1ca97145e838

  • NADAC price for package 64764075030

    GET /v1/drugs/nadac/64764075030

Use it

Look up 64764-750 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/64764-750 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 64764-750. 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.