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topiramate

NDC 71205-233, topiramate, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-233
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078235
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-233 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TOPIRAMATE25 mg/1

Pharmacologic classes

Cytochrome P450 2C19 Inhibitors [MoA]; Cytochrome P450 3A4 Inducers [MoA]; Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
71205-233-307120502333030 TABLET, FILM COATED in 1 BOTTLE (71205-233-30)
71205-233-607120502336060 TABLET, FILM COATED in 1 BOTTLE (71205-233-60)
71205-233-907120502339090 TABLET, FILM COATED in 1 BOTTLE (71205-233-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/80481455-7ad7-4f44-8113-b8b61d8581a0

Use it

Look up 71205-233 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-233 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-233. 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.