Levetiracetam
NDC 65162-539, Levetiracetam, tablet, film coated, from Amneal Pharmaceuticals LLC.
- Product NDC
- 65162-539
- Status
- Listed
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090767
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/65162-539 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LEVETIRACETAM1000 mg/1
Pharmacologic classes
Decreased Central Nervous System Disorganized Electrical Activity [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 65162-539-06 | 65162053906 | 60 TABLET, FILM COATED in 1 BOTTLE (65162-539-06) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/d7932a2c-a3b7-46df-a306-1f17716160a0
Use it
Look up 65162-539 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/65162-539 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 65162-539. 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.