NDC 50436-0387
Duloxetine 60 mg capsule, delayed release
On the label: Unit Dose Services. It's repackaged from NDC 68382-387, made by Zydus Pharmaceuticals USA 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 and relabels 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 Unit Dose Services names for other drugs.
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release
- Strength
- 60 mg
- Approval
- ANDA ANDA090739
- On the market since
- May 27, 2014
- Package NDCs
50436-0387-1- Official label
- DailyMed (National Library of Medicine), updated Oct 10, 2017
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?