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topiramate

NDC 82009-135, topiramate, tablet, film coated, from Quallent Pharmaceuticals Health LLC.

Product NDC
82009-135
Status
Listed
Labeler
Quallent Pharmaceuticals Health LLC
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/82009-135 \
  -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
82009-135-0582009013505500 TABLET, FILM COATED in 1 BOTTLE (82009-135-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9dae6824-6913-42de-b98a-cdcb0d3b4a46

  • NADAC price for package 82009013505

    GET /v1/drugs/nadac/82009013505

Use it

Look up 82009-135 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82009-135 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82009-135. 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.