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Oxcarbazepine

NDC 62756-183, Oxcarbazepine, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-183
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
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/62756-183 \
  -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
62756-183-0862756018308100 TABLET, FILM COATED in 1 BOTTLE (62756-183-08)
62756-183-836275601838330 TABLET, FILM COATED in 1 BOTTLE (62756-183-83)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7ecd5eef-46f4-407f-9b63-ba65adb3eced

Use it

Look up 62756-183 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-183 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-183. 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.