D-0305-2020 Class III Terminated

Recalled by Lupin Pharmaceuticals Inc. — Baltimore, MD

Recall Details

Product Type
Drugs
Report Date
November 13, 2019
Initiation Date
November 1, 2019
Termination Date
March 4, 2021
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
30,516 bottles

Product Description

Cefdinir for Oral Suspension USP, 250 mg/5mL,100 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, United States, Manufactured by: Lupin Limited, Mandideep 462 046 INDIA, NDC 68180-723-10

Reason for Recall

Presence of Foreign substance: identified as a dead ant.

Distribution Pattern

Product was distributed to major distributors/wholesalers throughout the United States.

Code Information

Lot #: F802345, F802346, F802347, Exp 11/20