NDC 70518-0937
Duloxetine 60 mg capsule, delayed release
On the label: Remedyrepack Inc.. It's repackaged from NDC 57237-019, 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. 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 Remedyrepack Inc. names for other drugs.
Recalls
- Dec 2, 2024 · Class II · RemedyRepack Inc.
CGMP Deviations; presence of N-nitroso-duloxetine impurity above recommended interim limit.
Lots: a) NDC 70518-0937-04, Lot # J0786744-061724, Exp. 06/30/2025 b) NDC 70518-0937-03, Lot # B3002625-060524, Exp. 10/31/2025
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release
- Strength
- 60 mg
- Approval
- ANDA ANDA090778
- On the market since
- Apr 25, 2019
- Package NDCs
70518-0937-070518-0937-170518-0937-270518-0937-370518-0937-470518-0937-570518-0937-670518-0937-7- Official label
- DailyMed (National Library of Medicine), updated Aug 7, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?