Levetiracetam
- Product NDC
- 70518-2230
- 11-digit product format
- 705182230
- Labeler code
- 70518
- Product ID
- 70518-2230_c7160c43-85d3-1cd5-e053-2995a90a4834
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090515
- Marketing category
- ANDA
- Marketing start
- 2019-07-23
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2230 | LEVETIRACETAM TABLET, FILM COATED [REMEDYREPACK INC.] | 8 | Legacy NDC | 20250309_03bbb88b-fe75-4b58-8cd4-1edbf8f284d4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2230-0 | 70518223000 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2230-0) | 2019-07-23 | 0000-00-00 | No | No | Current |