Levetiracetam
NDC 70010-522, Levetiracetam, tablet, film coated, from Granules Pharmaceuticals Inc..
- Product NDC
- 70010-522
- Status
- Listed
- Labeler
- Granules Pharmaceuticals Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA217878
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70010-522 \ -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 |
|---|---|---|
| 70010-522-03 | 70010052203 | 30 TABLET, FILM COATED in 1 BOTTLE (70010-522-03) |
| 70010-522-10 | 70010052210 | 1000 TABLET, FILM COATED in 1 BOTTLE (70010-522-10) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b4781ec4-43ad-4052-9a6a-b24fda119b32
Use it
Look up 70010-522 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70010-522 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70010-522. 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.