FDA Recalls Triple SupremeZen Plus 3500 for Unapproved Tadalafil
Hyobin LLC is recalling Triple SupremeZen Plus 3500 capsules because FDA analysis found the unapproved drug tadalafil. The product was marketed without an approved NDA or ANDA.
- Product
- Triple SupremeZen Plus 3500, packaged in cardboard blisters containing one capsule per card, Distributed by Yolo Studio, Cliffside Park, NJ
- Category
- Drug
- Distribution
- Distributed nationwide