Levetiracetam
- Product NDC
- 70518-0365
- 11-digit product format
- 705180365
- Labeler code
- 70518
- Product ID
- 70518-0365_83ee9883-a065-c7c0-e053-2a91aa0a6ac0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078106
- Marketing category
- ANDA
- Marketing start
- 2017-03-27
- 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
- 2020-12-31
- 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 |
|---|
| 70518-0365 | LEVETIRACETAM TABLET, FILM COATED [REMEDYREPACK INC.] | 9 | Legacy NDC | 20250426_743c6bda-f5e5-486b-bfed-11a72a5fb239.zip |