NDC 85534-0050
Duloxetine 20 mg capsule, delayed release pellets
On the label: Hawaii Repack, Inc.. It's repackaged: Hawaii Repack, Inc. rebottles it from Actavis Pharma, Inc.'s NDC 0228-2890.
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 Actavis Pharma, Inc. names for other drugs.
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release pellets, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA090776
- On the market since
- Dec 17, 2013
- Package NDCs
85534-0050-085534-0050-185534-0050-285534-0050-3- Official label
- DailyMed (National Library of Medicine), updated Sep 9, 2026
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