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Olanzapine

NDC 33342-085 · Macleods Pharmaceuticals Limited

Generic nameOlanzapine
Dosage formTABLET, ORALLY DISINTEGRATING
RouteORAL
Active ingredient(s)OLANZAPINE
Strength15 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

33342-085-07 — 30 TABLET, ORALLY DISINTEGRATING in 1 CONTAINER (33342-085-07)

33342-085-11 — 100 TABLET, ORALLY DISINTEGRATING in 1 CONTAINER (33342-085-11)

33342-085-12 — 10 BLISTER PACK in 1 CARTON (33342-085-12) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

33342-085-15 — 500 TABLET, ORALLY DISINTEGRATING in 1 CONTAINER (33342-085-15)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

13668-171 — OLANZAPINE, 31722-308 — Olanzapine, 33342-067 — Olanzapine, 33342-068 — Olanzapine, 33342-069 — Olanzapine, 33342-070 — Olanzapine, 33342-071 — Olanzapine, 33342-072 — Olanzapine, 33342-083 — Olanzapine, 33342-084 — Olanzapine, 33342-086 — Olanzapine, 39822-1800 — Olanzapine, 42291-652 — Olanzapine and Fluoxetine, 42291-653 — Olanzapine and Fluoxetine, 42291-654 — Olanzapine and Fluoxetine, 42291-655 — Olanzapine and Fluoxetine, 42291-656 — Olanzapine and Fluoxetine, 43598-164 — Olanzapine, 43598-165 — Olanzapine, 43598-166 — Olanzapine, +221 more

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