NDC 67046-1550
Olanzapine 5 mg tablet, orally disintegrating
On the label: Coupler LLC. It's repackaged: Coupler LLC 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
- Coupler LLC, West Chester, PA, United States · repackages 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
- Apr 9, 2025
- Package NDCs
67046-1550-3- Official label
- DailyMed (National Library of Medicine), updated Apr 9, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?