Levetiracetam
- Product NDC
- 35356-533
- 11-digit product format
- 353560533
- Labeler code
- 35356
- Product ID
- 35356-533_5a9345bb-8720-4184-aa87-35e09b538298
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA078154
- Marketing category
- ANDA
- Marketing start
- 2012-01-23
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 500 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 44YRR34555 | LEVETIRACETAM | 102767-28-2 | LEVETIRACETAM |