Levetiracetam
- Product NDC
- 68001-116
- 11-digit product format
- 680010116
- Labeler code
- 68001
- Product ID
- 68001-116_c4f8afaf-f30f-7a1f-e053-2995a90a05a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA078154
- Marketing category
- ANDA
- Marketing start
- 2014-02-24
- Marketing end
- 2022-11-30
- Substance
- LEVETIRACETAM
- Active strength
- 250 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68001-116-03 | 68001011603 | 500 TABLET, FILM COATED in 1 BOTTLE (68001-116-03) | 2014-02-24 | 2022-11-30 | No | No | Current |
| 68001-116-07 | 68001011607 | 120 TABLET, FILM COATED in 1 BOTTLE (68001-116-07) | 2014-02-24 | 2022-11-30 | No | No | Current |