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OXCARBAZEPINE

NDC 72189-339, OXCARBAZEPINE, tablet, film coated, from DirectRx.

Product NDC
72189-339
Status
Listed
Labeler
DirectRx
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077794
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-339 \
  -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
72189-339-607218903396060 TABLET, FILM COATED in 1 BOTTLE (72189-339-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dbea45c2-e166-b557-e053-2995a90a7643

Use it

Look up 72189-339 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-339 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-339. 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.