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SUBVENITE

NDC 69102-150 · OWP Pharmaceuticals, Inc.

Generic nameLAMOTRIGINE
Dosage formTABLET
RouteORAL
Active ingredient(s)LAMOTRIGINE
Strength150 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

69102-150-06 — 100 TABLET in 1 BOTTLE (69102-150-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68382-980 — Lamotrigine, 68382-981 — Lamotrigine, 68382-982 — Lamotrigine, 68382-983 — Lamotrigine, 68382-984 — Lamotrigine, 68462-228 — Lamotrigine, 68462-229 — Lamotrigine, 68788-7223 — Lamotrigine, 68788-7544 — Lamotrigine, 68788-7871 — Lamotrigine, 69102-301 — LAMOTRIGINE, 69102-319 — LAMOTRIGINE, 69102-320 — LAMOTRIGINE, 69102-418 — LAMOTRIGINE, 69102-639 — LAMOTRIGINE, 69117-0044 — lamotrigine extended-release, 69117-0045 — lamotrigine extended-release, 69117-0046 — lamotrigine extended-release, 69117-0047 — lamotrigine extended-release, 69117-0048 — lamotrigine extended-release, +270 more

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels