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Olanzapine

NDC 43598-165 · Dr. Reddy's Laboratories Inc.

Generic nameOlanzapine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)OLANZAPINE
Strength7.5 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

43598-165-01 — 100 TABLET, FILM COATED in 1 BOTTLE (43598-165-01)

43598-165-05 — 500 TABLET, FILM COATED in 1 BOTTLE (43598-165-05)

43598-165-30 — 30 TABLET, FILM COATED in 1 BOTTLE (43598-165-30)

43598-165-60 — 60 TABLET, FILM COATED in 1 BOTTLE (43598-165-60)

43598-165-78 — 10 BLISTER PACK in 1 CARTON (43598-165-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-165-79)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

33342-084 — Olanzapine, 33342-085 — 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, 43598-166 — Olanzapine, 49884-250 — olanzapine and fuoxetine, 49884-251 — olanzapine and fuoxetine, 49884-252 — olanzapine and fuoxetine, 49884-253 — olanzapine and fuoxetine, 49884-277 — olanzapine and fuoxetine, 51407-261 — Olanzapine, 51407-262 — Olanzapine, 51407-263 — Olanzapine, 51407-264 — 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.