Olanzapine 5 mg tablet, orally disintegrating

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Apotex Corp. names for other drugs.

Recalls

• Apr 7, 2015 · Class III · Apotex Inc.
  Subpotent drug
  Lots: Lot #: a) KL0655, Exp 04/15; KY2374, Exp 05/16; b) KL0656, Exp 04/15; KY2371, Exp 05/16
• Apr 18, 2014 · Class III · Apotex Corp.
  Subpotent Drug: Out of specification (OOS) results at the 9 month temperature point.
  Lots: Lot # KM4951; Exp. 04/15

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Olanzapine: every company that makes it

Form

tablet, orally disintegrating, oral

Strength

5 mg

Approval

ANDA ANDA091265

On the market since

Oct 24, 2011

Package NDCs

60505-3275-0 60505-3275-3 60505-3275-8

Official label

DailyMed (National Library of Medicine), updated Sep 15, 2026

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?