Lamotrigine
NDC 16714-893 · NorthStar Rx LLC
Generic nameLamotrigine
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)LAMOTRIGINE
Strength250 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
16714-893-01 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-893-01)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
16571-786 — Lamotrigine, 16714-194 — Lamotrigine, 16714-195 — Lamotrigine, 16714-196 — Lamotrigine, 16714-197 — Lamotrigine, 16714-623 — Lamotrigine, 16714-624 — Lamotrigine, 16714-625 — Lamotrigine, 16714-626 — Lamotrigine, 16714-627 — Lamotrigine, 27241-183 — Lamotrigine, 27241-184 — Lamotrigine, 27241-185 — Lamotrigine, 27241-186 — Lamotrigine, 29300-111 — Lamotrigine, 29300-112 — Lamotrigine, 29300-113 — Lamotrigine, 29300-114 — Lamotrigine, 31722-240 — lamotrigine extended-release, 31722-241 — lamotrigine extended-release, +270 more