NDC 71610-401
Duloxetine 20 mg capsule, delayed release
On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged from NDC 57237-017, made by Rising Pharma Holdings, Inc. (Duloxetine). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). 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 Aphena Pharma Solutions - Tennessee, Inc. names for other drugs.
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA090778
- On the market since
- Dec 11, 2013
- Package NDCs
71610-401-83- Official label
- DailyMed (National Library of Medicine), updated Mar 17, 2020
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