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topiramate

NDC 68071-3660, topiramate, tablet, film coated, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-3660
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090162
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3660 \
  -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
68071-3660-36807136600330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3660-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1ef1c408-30f7-51ee-e063-6394a90ac880

Use it

Look up 68071-3660 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3660 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-3660. 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.