Topiramate
NDC 47335-707, Topiramate, tablet, film coated, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 47335-707
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090278
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/47335-707 \ -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 NDC | NDC-11 | Package |
|---|---|---|
| 47335-707-08 | 47335070708 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-707-08) |
| 47335-707-18 | 47335070718 | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-707-18) |
| 47335-707-83 | 47335070783 | 30 TABLET, FILM COATED in 1 BOTTLE (47335-707-83) |
| 47335-707-86 | 47335070786 | 60 TABLET, FILM COATED in 1 BOTTLE (47335-707-86) |
| 47335-707-88 | 47335070788 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-707-88) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3c909a53-ae66-4b28-a741-b60bb25a69cfNADAC price for package 47335070786
GET /v1/drugs/nadac/47335070786
Use it
Look up 47335-707 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/47335-707 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 47335-707. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.