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Lamotrigine

NDC 13668-339 · Torrent Pharmaceuticals Limited

Generic nameLamotrigine
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)LAMOTRIGINE
Strength25 mg/1
Pharmacologic classAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Dihydrofolate Reductase Inhibitors [MoA], Mood Stabilizer [EPC], Organic Cation Transporter 2 Inhibitors [MoA]
Marketing categoryANDA

Packages

13668-339-01 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-339-01)

13668-339-05 — 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-339-05)

13668-339-30 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-339-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0904-7007 — Lamotrigine, 0904-7008 — Lamotrigine, 10370-207 — lamotrigine, 10370-208 — lamotrigine, 10370-256 — lamotrigine, 10370-334 — lamotrigine, 13668-045 — LAMOTRIGINE, 13668-047 — LAMOTRIGINE, 13668-048 — LAMOTRIGINE, 13668-049 — LAMOTRIGINE, 13668-340 — Lamotrigine, 13668-341 — Lamotrigine, 13668-693 — LAMOTRIGINE, 13668-694 — LAMOTRIGINE, 13668-695 — LAMOTRIGINE, 13668-696 — LAMOTRIGINE, 16571-785 — Lamotrigine, 16571-786 — Lamotrigine, 16714-194 — Lamotrigine, 16714-195 — Lamotrigine, +270 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.