Levetiracetam
- Product NDC
- 68788-6798
- 11-digit product format
- 687886798
- Labeler code
- 68788
- Product ID
- 68788-6798_235f30aa-1f38-45af-b18f-9a91eb58063c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA090843
- Marketing category
- ANDA
- Marketing start
- 2016-11-03
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 250 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record