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Topiramate

NDC 70518-4340, Topiramate, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-4340
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077627
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4340 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TOPIRAMATE50 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
70518-4340-070518434000100 POUCH in 1 BOX (70518-4340-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4340-1)
70518-4340-27051843400230 POUCH in 1 BOX (70518-4340-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-4340-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3f99b26b-79b9-4efb-aa2c-2868e1e126c8

Use it

Look up 70518-4340 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4340 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4340. 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.