Amoxicillin for Oral Suspension, USP 400mg/5mL, NDC 0093-4161-78 (75ml) and 0093-4161-73 (100mL)
Recall Number: D-598-2013
Firm: Teva Pharmaceuticals USA, Inc.
Classification: Class III
Status: Terminated
Report Date: 20130619
Initiation Date: 20130426
Termination Date: 20131224
Reason for Recall
Discoloration: This recall is being carried out due to a yellow to brown discolored Amoxicillin powder on the inner foil seal of the bottles.
Product Description
Amoxicillin for Oral Suspension, USP 400mg/5mL, NDC 0093-4161-78 (75ml) and 0093-4161-73 (100mL)