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Oxcarbazepine

NDC 59651-785, Oxcarbazepine, tablet, film coated, extended release, from Aurobindo Pharma Limited.

Product NDC
59651-785
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219241
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-785 \
  -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
59651-785-0159651078501100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-785-01)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/21caded0-2ed7-4f7d-9856-27ef7c1a47c8

Use it

Look up 59651-785 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-785 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-785. 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.