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Oxcarbazepine

NDC 60290-067, Oxcarbazepine, tablet, film coated, from Umedica Laboratories USA Inc..

Product NDC
60290-067
Status
Listed
Labeler
Umedica Laboratories USA Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218341
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60290-067 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXCARBAZEPINE150 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
60290-067-0160290006701100 TABLET, FILM COATED in 1 BOTTLE (60290-067-01)
60290-067-0260290006702500 TABLET, FILM COATED in 1 BOTTLE (60290-067-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e46d4654-76bc-4c33-ac2b-e89ae11b7697

Use it

Look up 60290-067 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60290-067 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60290-067. 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.