LEVETIRACETAM
- Product NDC
- 61919-559
- 11-digit product format
- 619190559
- Labeler code
- 61919
- Product ID
- 61919-559_ea4ea5a1-3101-d5dd-e053-2995a90ab48c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LEVETIRACETAM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA078106
- Marketing category
- ANDA
- Marketing start
- 2019-08-29
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-559-60 | 61919055960 | 60 TABLET, FILM COATED in 1 BOTTLE (61919-559-60) | 2019-04-17 | 0000-00-00 | No | No | Current |
| 61919-559-90 | 61919055990 | 90 TABLET, FILM COATED in 1 BOTTLE (61919-559-90) | 2019-08-29 | 0000-00-00 | No | No | Current |