Levetiracetam
- Product NDC
- 42385-957
- 11-digit product format
- 423850957
- Labeler code
- 42385
- Product ID
- 42385-957_cbdae2e4-1013-e3d8-e053-2995a90a625c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Laurus Generics Inc.
- Application
- ANDA090767
- Marketing category
- ANDA
- Marketing start
- 2021-03-22
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 1000 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42385-957 | LEVETIRACETAM TABLET [LAURUS GENERICS INC.] | 3 | Legacy NDC | 20250121_6c7d64d6-1105-4eb6-abaf-bc41fdfe00bd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42385-957-60 | 42385095760 | 60 TABLET in 1 BOTTLE (42385-957-60) | 60 tablet | 2021-03-22 | 0000-00-00 | No | No | Current |