NDC 87063-702
Duloxetine 20 mg capsule, delayed release
On the label: Asclemed USA, Inc..
FDA lists this product, but its label isn't on DailyMed yet, so we can't show its factories. They usually appear within a few weeks.
Where it's made
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA208706
- On the market since
- Mar 16, 2017
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