NDC 71335-0830 – Lamotrigine
Lamotrigine 200 mg/1 · Tablet · Oral
Product NDC71335-0830
Product details
- Brand name
- Lamotrigine
- Generic name
- Lamotrigine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA090170
- Marketed since
- November 1, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Lamotrigine 200 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0830-1 | 30 TABLET in 1 BOTTLE (71335-0830-1) | Feb 9, 2022 |
| 71335-0830-2 | 60 TABLET in 1 BOTTLE (71335-0830-2) | Feb 9, 2022 |
| 71335-0830-3 | 90 TABLET in 1 BOTTLE (71335-0830-3) | Feb 9, 2022 |
| 71335-0830-4 | 45 TABLET in 1 BOTTLE (71335-0830-4) | Feb 9, 2022 |
| 71335-0830-5 | 180 TABLET in 1 BOTTLE (71335-0830-5) | Feb 9, 2022 |
| 71335-0830-6 | 14 TABLET in 1 BOTTLE (71335-0830-6) | Feb 9, 2022 |
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