Levetiracetam
- Product NDC
- 70518-0947
- 11-digit product format
- 705180947
- Labeler code
- 70518
- Product ID
- 70518-0947_e9e61a32-d816-2fa3-e053-2a95a90a63ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090515
- Marketing category
- ANDA
- Marketing start
- 2018-01-10
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 250 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0947 | LEVETIRACETAM TABLET, FILM COATED [REMEDYREPACK INC.] | 16 | Legacy NDC | 20250504_1f4a0acc-d5f5-438d-96a0-897dfebdf6e4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0947-1 | 70518094701 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0947-1) | 2020-05-28 | 0000-00-00 | No | No | Current |