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Topiramate

NDC 71205-214, Topiramate, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-214
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090278
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-214 \
  -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
71205-214-307120502143030 TABLET, FILM COATED in 1 BOTTLE (71205-214-30)
71205-214-607120502146060 TABLET, FILM COATED in 1 BOTTLE (71205-214-60)
71205-214-907120502149090 TABLET, FILM COATED in 1 BOTTLE (71205-214-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e382a731-ef73-4990-bc74-ffc3a91ff3ba

Use it

Look up 71205-214 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-214 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-214. 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.