topiramate
NDC 70518-1180, topiramate, tablet, film coated, from REMEDYREPACK INC..
- Product NDC
- 70518-1180
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078235
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1180 \ -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 NDC | NDC-11 | Package |
|---|---|---|
| 70518-1180-3 | 70518118003 | 30 POUCH in 1 BOX (70518-1180-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-1180-2) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2f5b1b0b-fd8a-4c4e-a85a-519ca841a0db
Use it
Look up 70518-1180 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1180 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-1180. 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.