NDC 0173-0633 – Lamictal
Lamotrigine 25 mg/1 · Tablet · Oral
Product NDC0173-0633
Product details
- Brand name
- Lamictal
- Generic name
- Lamotrigine
- Labeler
- GlaxoSmithKline LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- NDA · NDA020241
- Marketed since
- August 15, 1996
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Lamotrigine 25 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0173-0633-02 | 100 TABLET in 1 BOTTLE (0173-0633-02) | Aug 15, 1996 |
| 0173-0633-10 | 35 TABLET in 1 DOSE PACK (0173-0633-10) | Aug 15, 1996 |
Other Lamictal products
- 0173-0642 Lamotrigine 100 mg/1 · Tablet · GlaxoSmithKline LLC
- 0173-0643 Lamotrigine 150 mg/1 · Tablet · GlaxoSmithKline LLC
- 0173-0644 Lamotrigine 200 mg/1 · Tablet · GlaxoSmithKline LLC
- 0173-0526 Lamotrigine 5 mg/1 · Tablet, For Suspension · GlaxoSmithKline LLC
- 0173-0527 Lamotrigine 25 mg/1 · Tablet, For Suspension · GlaxoSmithKline LLC
- 0173-0594 · Kit · GlaxoSmithKline LLC
- 0173-0699 Lamotrigine 2 mg/1 · Tablet, For Suspension · GlaxoSmithKline LLC
- 0173-0754 Lamotrigine 25 mg/1 · Tablet, Film Coated, Extended Release · GlaxoSmithKline LLC
- 0173-0755 Lamotrigine 50 mg/1 · Tablet, Film Coated, Extended Release · GlaxoSmithKline LLC
- 0173-0756 Lamotrigine 100 mg/1 · Tablet, Film Coated, Extended Release · GlaxoSmithKline LLC
- 0173-0757 Lamotrigine 200 mg/1 · Tablet, Film Coated, Extended Release · GlaxoSmithKline LLC
- 0173-0758 · Kit · GlaxoSmithKline LLC