Lamotrigine 51672-4252
Product NDC
51672-4252- 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
Need to source Lamotrigine? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
Active Ingredients
| Ingredient | Strength |
|---|---|
| Lamotrigine | 25 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Mood Stabilizer [EPC]Anti-epileptic Agent [EPC]
Packaging Options(1)
30 TABLET in 1 BOTTLE (51672-4252-6)