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Oxcarbazepine

NDC 62559-220, Oxcarbazepine, tablet, film coated, from ANI Pharmaceuticals, Inc..

Product NDC
62559-220
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078005
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62559-220 \
  -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
62559-220-0162559022001100 TABLET, FILM COATED in 1 BOTTLE (62559-220-01)
62559-220-0562559022005500 TABLET, FILM COATED in 1 BOTTLE (62559-220-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/867eaf99-3e31-4f75-bfae-2898804d956d

  • NADAC price for package 62559022001

    GET /v1/drugs/nadac/62559022001

Use it

Look up 62559-220 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62559-220 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62559-220. 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.