NDC 80175-0582
duloxetine 30 mg capsule, delayed release
On the label: Central Packaging. It's repackaged from NDC 31722-582, made by Camber Pharmaceuticals, 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 Central Packaging names for other drugs.
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release
- Strength
- 30 mg
- Approval
- ANDA ANDA204343
- On the market since
- Aug 11, 2016
- Package NDCs
80175-0582-3- Official label
- DailyMed (National Library of Medicine), updated Mar 8, 2021
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