NDC 21695-229
Lamotrigine 200 mg tablet
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-4133.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Taro Pharmaceutical Industries Ltd. | Haifa Bay, Israel | Makes it | No problems foundDec 8, 2022 · 7 inspections |
Recalls
- Dec 20, 2019 · Class I · Taro Pharmaceuticals U.S.A., Inc.
Cross Contamination; Lamotrigine Tablets 100 mg USP was contaminated with enalapril maleate.
Lots: Lot #: 331771, Exp. June 2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Lamotrigine: every company that makes it
- Form
- tablet
- Strength
- 200 mg
- Approval
- NDA NDA078525
- On the market since
- Jan 27, 2009
- Package NDCs
21695-229-60- Official label
- DailyMed (National Library of Medicine), updated Sep 30, 2010
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