Duloxetine delayed-release capsules exceed the interim limit for a nitrosamine impurity
Duloxetine Delayed-Release Capsules 40 mg are being recalled because N-nitroso-duloxetine was present above the FDA recommended interim limit. 12,242 bottles are affected.
- Product
- DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
- Category
- Drug
- Distribution
- Distributed nationwide