levetiracetam
- Product NDC
- 10370-214
- 11-digit product format
- 103700214
- Labeler code
- 10370
- Product ID
- 10370-214_a46e7248-dd69-4781-98a2-e08646630304
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levetiracetam
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA091360
- Marketing category
- ANDA
- Marketing start
- 2011-10-04
- 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
- 2020-12-31
- 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 |
|---|
| 10370-214-06 | 10370021406 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10370-214-06) | 2011-10-04 | 0000-00-00 | No | No | Current |
| 10370-214-09 | 10370021409 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10370-214-09) | 2011-10-04 | 0000-00-00 | No | No | Current |
| 10370-214-50 | 10370021450 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10370-214-50) | 2011-10-04 | 0000-00-00 | No | No | Current |