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NDC 70518-4483, vortioxetine, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-4483
Status
Listed
Labeler
REMEDYREPACK 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/70518-4483 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VORTIOXETINE HYDROBROMIDE5 mg/1
Package NDCNDC-11Package
70518-4483-07051844830030 POUCH in 1 BOX (70518-4483-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4483-1)
70518-4483-27051844830250 POUCH in 1 BOX (70518-4483-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-4483-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bd0107e5-1cb9-4b40-a6af-fa65fcbe6b4e

Use it

Look up 70518-4483 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4483 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4483. 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.