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OXCARBAZEPINE

NDC 51991-293, OXCARBAZEPINE, tablet, film coated, from Breckenridge Pharmaceutical, Inc..

Product NDC
51991-293
Status
Listed
Labeler
Breckenridge Pharmaceutical, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078069
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51991-293 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXCARBAZEPINE300 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51991-293-0151991029301100 TABLET, FILM COATED in 1 BOTTLE (51991-293-01)
51991-293-0551991029305500 TABLET, FILM COATED in 1 BOTTLE (51991-293-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/682a1210-b26e-426e-8ffe-d25d91bdd608

  • NADAC price for package 51991029301

    GET /v1/drugs/nadac/51991029301

  • NADAC price for package 51991029305

    GET /v1/drugs/nadac/51991029305

Use it

Look up 51991-293 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51991-293 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51991-293. 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.