NDC 80425-0014
Duloxetine HCLDR 30 mg capsule, delayed release
On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged from NDC 57237-018, made by Rising Pharma Holdings, 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 Advanced Rx Pharmacy of Tennessee, LLC names for other drugs.
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA090778
- On the market since
- Dec 11, 2022
- Package NDCs
80425-0014-180425-0014-2- Official label
- DailyMed (National Library of Medicine), updated Dec 31, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?