Levetiracetam
- Product NDC
- 68788-7190
- 11-digit product format
- 687887190
- Labeler code
- 68788
- Product ID
- 68788-7190_115cefe3-28c3-4388-8ec5-b417e6dc792b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA078154
- Marketing category
- ANDA
- Marketing start
- 2018-07-17
- 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#