Levetiracetam
- Product NDC
- 70518-0648
- 11-digit product format
- 705180648
- Labeler code
- 70518
- Product ID
- 70518-0648_884098bb-2a92-6029-e053-2a95a90a24c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091399
- Marketing category
- ANDA
- Marketing start
- 2017-07-28
- 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
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record