Lamotrigine 51672-4255
Product NDC
51672-4255- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 27, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA219677
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lamotrigine | 200 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Mood Stabilizer [EPC]Anti-epileptic Agent [EPC]
Packaging Options(1)
30 TABLET in 1 BOTTLE (51672-4255-6)