Levetiracetam
- Product NDC
- 71930-063
- 11-digit product format
- 719300063
- Labeler code
- 71930
- Product ID
- 71930-063_bc9d8d29-4a90-6efc-e053-2a95a90a0ff2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- EYWA Pharma Inc.
- Application
- ANDA090767
- Marketing category
- ANDA
- Marketing start
- 2019-12-05
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71930-063-15 | 71930006315 | 120 TABLET in 1 BOTTLE (71930-063-15) | 120 tablet | 2019-12-05 | 0000-00-00 | No | No | Current |
| 71930-063-52 | 71930006352 | 500 TABLET in 1 BOTTLE (71930-063-52) | 500 tablet | 2019-12-05 | 0000-00-00 | No | No | Current |