Levetiracetam
- Product NDC
- 0228-2167
- 11-digit product format
- 002282167
- Labeler code
- 0228
- Product ID
- 0228-2167_eaa14eb1-3ca5-4803-9bf7-8fb5766dd373
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Actavis Elizabeth LLC
- Application
- ANDA090484
- Marketing category
- ANDA
- Marketing start
- 2011-04-04
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#