NDC 51407-261
Olanzapine 5 mg tablet, orally disintegrating
On the label: Golden State Medical Supply, Inc.. It's repackaged: Golden State Medical Supply, Inc. rebottles it from Apotex Corp.'s NDC 60505-3275.
Where the pills inside were 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.
Repackaging site
- Golden State Medical Supply Inc., Camarillo, CA, United States · repackages it and relabels it
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
51407-261-30- Official label
- DailyMed (National Library of Medicine), updated Apr 15, 2025
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