NDC 0378-5617 – Levetiracetam
Levetiracetam 750 mg/1 · Tablet, Film Coated · Oral
Product NDC0378-5617
Product details
- Brand name
- Levetiracetam
- Generic name
- Levetiracetam
- Labeler
- Mylan Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076919
- Marketed since
- November 4, 2008
- Listing expires
- December 31, 2026
Active ingredients
- Levetiracetam 750 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0378-5617-05 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5617-05) | Nov 4, 2008 |
| 0378-5617-78 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5617-78) | Nov 4, 2008 |
Recalls mentioning this NDC
- D-1702-2012 Oct 3, 2012 · Class II
Adulterated Presence of Foreign Tablets: Pharmaceutical manufacturer may have distributed foreign tablets in bottles of Levetiracetam Tablets, USP 500 mg.
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