NDC 51672-4133 – Lamotrigine
Lamotrigine 200 mg/1 · Tablet · Oral
Product NDC51672-4133
Product details
- Brand name
- Lamotrigine
- Generic name
- Lamotrigine
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078525
- Marketed since
- January 27, 2009
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Lamotrigine 200 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4133-0 | 10 BLISTER PACK in 1 CARTON (51672-4133-0) / 10 TABLET in 1 BLISTER PACK | Jan 27, 2009 |
| 51672-4133-1 | 100 TABLET in 1 BOTTLE (51672-4133-1) | Jan 27, 2009 |
| 51672-4133-3 | 1000 TABLET in 1 BOTTLE (51672-4133-3) | Jan 27, 2009 |
| 51672-4133-4 | 60 TABLET in 1 BOTTLE (51672-4133-4) | Jan 27, 2009 |
| 51672-4133-6 | 30 TABLET in 1 BOTTLE (51672-4133-6) | Jan 27, 2009 |
Recalls mentioning this NDC
- D-0833-2020 Feb 19, 2020 · Class I
Cross Contamination; Lamotrigine Tablets 100 mg USP was contaminated with enalapril maleate.
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