NDC 50436-2995
Duloxetine Hydrochloride 20 mg capsule, delayed release
On the label: Unit Dose Services. It's repackaged from NDC 60505-2995, made by Apotex Corp. (Duloxetine Hydrochloride). 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
- 20 mg
- Approval
- ANDA ANDA202045
- On the market since
- Jun 13, 2014
- Package NDCs
50436-2995-2- Official label
- DailyMed (National Library of Medicine), updated Feb 11, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?