Levetiracetam
- Product NDC
- 49884-204
- 11-digit product format
- 498840204
- Labeler code
- 49884
- Product ID
- 49884-204_8b278c49-8e40-4873-b73d-d5a4a3d6ee3a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levetiracetam
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Par Pharmaceutical Inc.
- Application
- ANDA091291
- Marketing category
- ANDA
- Marketing start
- 2011-09-13
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 500 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record