Levetiracetam
- Product NDC
- 70518-3534
- 11-digit product format
- 705183534
- Labeler code
- 70518
- Product ID
- 70518-3534_f0d4e8ab-be50-73f8-e053-2a95a90a5db4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078976
- Marketing category
- ANDA
- Marketing start
- 2022-09-23
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 100 mg/mL
- 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 |
|---|
| 70518-3534-0 | 70518353400 | 10 CUP, UNIT-DOSE in 1 BOX (70518-3534-0) > 5 mL in 1 CUP, UNIT-DOSE (70518-3534-1) | 2022-09-23 | 0000-00-00 | No | No | Current |