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Oxcarbazepine

NDC 71205-411, Oxcarbazepine, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-411
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077802
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-411 \
  -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
71205-411-307120504113030 TABLET, FILM COATED in 1 BOTTLE (71205-411-30)
71205-411-607120504116060 TABLET, FILM COATED in 1 BOTTLE (71205-411-60)
71205-411-907120504119090 TABLET, FILM COATED in 1 BOTTLE (71205-411-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/95867dcd-fd0e-4570-987b-d35939f7d7d1

Use it

Look up 71205-411 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-411 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-411. 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.