Levetiracetam
- Product NDC
- 52343-070
- 11-digit product format
- 523430070
- Labeler code
- 52343
- Product ID
- 52343-070_b3cc95a0-a119-4799-b6e3-714a07e36efb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ACETRIS HEALTH, LLC
- Application
- ANDA078993
- Marketing category
- ANDA
- Marketing start
- 2014-11-06
- 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
- 2020-12-31
- 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 |
|---|
| 52343-070-05 | 52343007005 | 500 TABLET, FILM COATED in 1 BOTTLE (52343-070-05) | 2014-11-06 | 0000-00-00 | No | No | Current |
| 52343-070-12 | 52343007012 | 120 TABLET, FILM COATED in 1 BOTTLE (52343-070-12) | 2014-11-06 | 0000-00-00 | No | No | Current |