Levetiracetam
NDC 70518-1796, Levetiracetam, tablet, film coated, from REMEDYREPACK INC..
- Product NDC
- 70518-1796
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090515
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1796 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LEVETIRACETAM500 mg/1
Pharmacologic classes
Decreased Central Nervous System Disorganized Electrical Activity [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-1796-2 | 70518179602 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1796-2) |
| 70518-1796-4 | 70518179604 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1796-4) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/dfc218c5-672a-420a-b59e-2e0b054e99ad
Use it
Look up 70518-1796 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1796 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-1796. 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.