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NDC 70518-4284, vortioxetine, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-4284
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/70518-4284 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VORTIOXETINE HYDROBROMIDE10 mg/1
Package NDCNDC-11Package
70518-4284-07051842840030 POUCH in 1 BOX (70518-4284-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4284-1)
70518-4284-27051842840250 POUCH in 1 BOX (70518-4284-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-4284-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/239215eb-be32-4286-9677-1e5556c6cccf

Use it

Look up 70518-4284 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4284 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4284. 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.