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Oxcarbazepine

NDC 50268-681, Oxcarbazepine, tablet, film coated, from AvPAK.

Product NDC
50268-681
Status
Listed
Labeler
AvPAK
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215939
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50268-681 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXCARBAZEPINE600 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
50268-681-155026806811550 BLISTER PACK in 1 BOX (50268-681-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-681-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fd8da0e9-d69b-7587-e053-6294a90a33c0

  • NADAC price for package 50268068115

    GET /v1/drugs/nadac/50268068115

Use it

Look up 50268-681 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50268-681 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50268-681. 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.