FDA Recalls Nitrofurantoin Capsules Due to Failed Dissolution Specifications
Sun Pharmaceutical recalls Nitrofurantoin Capsules (100 mg) due to failed dissolution, affecting medication effectiveness. The recall involves 5,752 bottles nationwide in lots 231067 and 231069.
- Product
- NITROFURANTION — NITROFURANTION (NITROFURANTION)
- Category
- Drug
- Distribution
- Distributed nationwide