Olanzapine

NDC 0093-5245 · Teva Pharmaceuticals USA, Inc.

Generic nameOlanzapine

Dosage formTABLET, ORALLY DISINTEGRATING

RouteORAL

Active ingredient(s)OLANZAPINE

Strength5 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

0093-5245-65 — 30 BLISTER PACK in 1 CARTON (0093-5245-65) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0093-5245-19)

FDA lists these products with the same active ingredient.

0093-5246 — Olanzapine, 0093-5247 — Olanzapine, 0093-5248 — Olanzapine, 0093-5503 — Olanzapine and Fluoxetine, 0093-5504 — Olanzapine and Fluoxetine, 0093-5505 — Olanzapine and Fluoxetine, 0093-5506 — Olanzapine and Fluoxetine, 0093-5507 — Olanzapine and Fluoxetine, 0121-1072 — Olanzapine, 0143-9199 — Olanzapine, 0517-0955 — Olanzapine, 0527-3161 — Olanzapine, 0527-3162 — Olanzapine, 0527-3163 — Olanzapine, 0527-3164 — Olanzapine, 0615-8243 — Olanzapine, 0615-8244 — Olanzapine, 0615-8245 — Olanzapine, 0615-8246 — Olanzapine, 0615-8566 — Olanzapine, +221 more

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