Levetiracetam
- Product NDC
- 16714-356
- 11-digit product format
- 167140356
- Labeler code
- 16714
- Product ID
- 16714-356_4d3e5006-b3fc-4987-a9a6-e15dceff384a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NorthStar Rx LLC
- Application
- ANDA078993
- Marketing category
- ANDA
- Marketing start
- 2009-01-15
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 750 mg/1
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 16714-356 | LEVETIRACETAM TABLET, FILM COATED [NORTHSTAR RX LLC] | 22 | Legacy NDC | 20240723_e77eabc9-9f65-4d4b-8135-0290291e6ee8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-356-01 | 16714035601 | 120 TABLET, FILM COATED in 1 BOTTLE (16714-356-01) | 2009-01-15 | 0000-00-00 | No | No | Current |
| 16714-356-02 | 16714035602 | 500 TABLET, FILM COATED in 1 BOTTLE (16714-356-02) | 2009-01-15 | 0000-00-00 | No | No | Current |