Levetiracetam
- Product NDC
- 70518-1998
- 11-digit product format
- 705181998
- Labeler code
- 70518
- Product ID
- 70518-1998_d7c0971b-bba9-74cf-e053-2a95a90a1eeb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090025
- Marketing category
- ANDA
- Marketing start
- 2019-04-02
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 1000 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 table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1998-0 | 70518199800 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1998-0) | 2019-04-02 | 0000-00-00 | No | No | Current |