LEVETIRACETAM
NDC 72189-229, LEVETIRACETAM, tablet, film coated, from DIRECT RX.
- Product NDC
- 72189-229
- Status
- Listed
- Labeler
- DIRECT RX
- 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/72189-229 \ -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 |
|---|---|---|
| 72189-229-60 | 72189022960 | 60 TABLET, FILM COATED in 1 BOTTLE (72189-229-60) |
| 72189-229-90 | 72189022990 | 90 TABLET, FILM COATED in 1 BOTTLE (72189-229-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c3b62114-a590-f4db-e053-2995a90a9d30
Use it
Look up 72189-229 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72189-229 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72189-229. 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.