Keppra
- Product NDC
- 65084-457
- 11-digit product format
- 650840457
- Labeler code
- 65084
- Product ID
- 65084-457_ef7f5ccc-c93b-47b3-a915-3e76610073a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mckesson Rxpak Inc
- Application
- NDA021035
- Marketing category
- NDA
- Marketing start
- 2000-04-24
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 750 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#