Levetiracetam
- Product NDC
- 0615-7978
- 11-digit product format
- 006157978
- Labeler code
- 0615
- Product ID
- 0615-7978_b1888f15-4a0c-4ff9-bc48-d27959ff1c1f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA090515
- Marketing category
- ANDA
- Marketing start
- 2012-01-09
- 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
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0615-7978-30 | 00615797830 | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7978-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK | 6 blister pack | 2016-08-23 | 0000-00-00 | No | No | Current |
| 0615-7978-39 | 00615797839 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7978-39) | 2016-05-18 | 0000-00-00 | No | No | Current |