LEVETIRACETAM
- Product NDC
- 63739-019
- 11-digit product format
- 637390019
- Labeler code
- 63739
- Product ID
- 63739-019_1d3d316a-4d83-48b7-b701-79b54ffcccf8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levetiracetam
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- McKesson Corporation DBA SKY Packaging
- Application
- ANDA079063
- Marketing category
- ANDA
- Marketing start
- 2021-06-01
- 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
- 2022-12-31
- 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 |
|---|
| 63739-019-71 | 63739001971 | 40 CUP, UNIT-DOSE in 1 CASE (63739-019-71) > 5 mL in 1 CUP, UNIT-DOSE (63739-019-70) | 2021-06-01 | 0000-00-00 | No | No | Current |