April 12, 2001Inderide LA Capsules Recalled by
Puerto Rico (SafetyAlerts) - The
Food and Drug Administration (FDA) said today that Wyeth Pharmaceuticals Company has
recalled certain Inderide LA 160 mg/50 mg caps because of dissolution failure for
This is the first public notice of
this Class III
recall issued by FDA.
Inderide LA 160 mg/50 mg caps (Propranolol HCL 160 mg/Hydrochlorothiazdie 50 mg),
NDC 0046-0459-81, bottles of 100 caps. 24 bottles of 100's per shipper.
Lot no. 999041 exp. date 7/01.
Wyeth Pharmaceuticals Company, Guayama, PR.
Manufacturer, by letters dated 2/28/01. Firm-initiated recall ongoing.
5, 576 bottles of 100.
Questions concerning this recall may be directed
to the FDA at 1-888-INFO-FDA.
Notice of this product warning was sent via email
to SafetyAlerts subscribers April
12, 2001. For more information regarding the SafetyAlerts free email alert service
please click here.