NDC 50090-7397
atomoxetine 60 mg capsule
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-269.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Goa, India | Makes it and tests it | Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · relabels it
Recalls
- Jan 29, 2025 · Class II · Glenmark Pharmaceuticals Inc., USA
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
Lots: Lot Numbers: 19234630, Exp.: 10/2025; 19240528, 19240529, Exp.: 1/2026.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Atomoxetine: every company that makes it
- Form
- capsule, oral
- Strength
- 60 mg
- Approval
- ANDA ANDA079019
- On the market since
- May 30, 2017
- Package NDCs
50090-7397-0- Official label
- DailyMed (National Library of Medicine), updated Oct 25, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?