Levetiracetam
- Product NDC
- 70518-2810
- 11-digit product format
- 705182810
- Labeler code
- 70518
- Product ID
- 70518-2810_d733a6d2-9d8c-1c77-e053-2995a90a6548
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204312
- Marketing category
- ANDA
- Marketing start
- 2020-07-10
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 500 mg/5mL
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2810-0 | 70518281000 | 10 VIAL, SINGLE-DOSE in 1 CARTON (70518-2810-0) > 5 mL in 1 VIAL, SINGLE-DOSE (70518-2810-1) | 2020-07-10 | 0000-00-00 | No | No | Current |