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Topiramate

NDC 65862-171, Topiramate, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-171
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078462
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-171 \
  -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
65862-171-0565862017105500 TABLET, FILM COATED in 1 BOTTLE (65862-171-05)
65862-171-606586201716060 TABLET, FILM COATED in 1 BOTTLE (65862-171-60)
65862-171-99658620171991000 TABLET, FILM COATED in 1 BOTTLE (65862-171-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/32b48ea0-a215-43b8-83b4-a5435a686d68

  • NADAC price for package 65862017160

    GET /v1/drugs/nadac/65862017160

Use it

Look up 65862-171 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-171 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-171. 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.