Levetiracetam
- Product NDC
- 70518-0430
- 11-digit product format
- 705180430
- Labeler code
- 70518
- Product ID
- 70518-0430_850019f4-c310-d29b-e053-2a91aa0a47c7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076919
- Marketing category
- ANDA
- Marketing start
- 2017-04-17
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 44YRR34555 | LEVETIRACETAM | 102767-28-2 | LEVETIRACETAM |