Glenmark Pharmaceuticals Inc., USA 2025-02-26 Health serious FDA
Health · FDA · Recall #FDA-D-0236-2025
Atomoxetine Capsules, USP, 80 mg, 30 capsule bottles, Rx Only, Manufactured for: Glenmark… Recall
Issued February 26, 2025 · Glenmark Pharmaceuticals Inc., USA
In February 2025, Glenmark Pharmaceuticals Inc., USA recalled the Atomoxetine Capsules, USP, 80 mg, 30 capsule bottles, Rx Only, Manufactured for: Glenmark…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
What you should do
- 1 Stop using Atomoxetine Capsules, USP, 80 mg, 30 capsule bottles, Rx Only, Manufactured for: Glenmark… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Glenmark Pharmaceuticals Inc., USA to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Glenmark Pharmaceuticals Inc., USA
- Category
- Health
- Recall date
- February 26, 2025
- Units affected
- Not reported
- Sold at
- Nationwide within the U.S
- Recall number
- FDA-D-0236-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Glenmark Pharmaceuticals Inc., USA has 53 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.