Topiramate
NDC 47335-712, Topiramate, tablet, film coated, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 47335-712
- 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/47335-712 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TOPIRAMATE200 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 |
|---|---|---|
| 47335-712-08 | 47335071208 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-712-08) |
| 47335-712-13 | 47335071213 | 500 TABLET, FILM COATED in 1 BOTTLE (47335-712-13) |
| 47335-712-18 | 47335071218 | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-712-18) |
| 47335-712-83 | 47335071283 | 30 TABLET, FILM COATED in 1 BOTTLE (47335-712-83) |
| 47335-712-86 | 47335071286 | 60 TABLET, FILM COATED in 1 BOTTLE (47335-712-86) |
| 47335-712-88 | 47335071288 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-712-88) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3c909a53-ae66-4b28-a741-b60bb25a69cf
Use it
Look up 47335-712 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/47335-712 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 47335-712. 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.