NDC 50436-0018
Duloxetine Hydrochloride 30 mg capsule, delayed release
On the label: Unit Dose Services.
It's a repackaged product (source NDC 57237-018, which isn't on a current label).
Where it's made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it and relabels it). Companies aren't required to print it on the label. The manufacturer's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Unit Dose Services uses for other drugs.
Product details
- Generic drug
- Duloxetine: see every company that makes it
- Form
- capsule, delayed release
- Strength
- 30 mg
- Approval
- ANDA ANDA090778
- On the market since
- Dec 11, 2013
- Package NDCs
50436-0018-150436-0018-2- Official label
- DailyMed (National Library of Medicine), updated Aug 14, 2017
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?