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topiramate

NDC 50090-2102, topiramate, tablet, film coated, from A-S Medication Solutions.

Product NDC
50090-2102
Status
Listed
Labeler
A-S Medication Solutions
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/50090-2102 \
  -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
50090-2102-05009021020060 TABLET, FILM COATED in 1 BOTTLE (50090-2102-0)
50090-2102-15009021020190 TABLET, FILM COATED in 1 BOTTLE (50090-2102-1)
50090-2102-25009021020230 TABLET, FILM COATED in 1 BOTTLE (50090-2102-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a5cffe7a-fdee-487a-bafb-a2d43e76c23c

Use it

Look up 50090-2102 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-2102 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-2102. 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.