Class II
Terminated
Cefdinir for Oral Suspension USP, 250 mg/5mL, packaged in 60 mL bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland, Manufactured by: Lupin Limited, Mandideep, India, NDC 68180-723-20
- Company
- Lupin Pharmaceuticals Inc.
- Recall Initiated
- July 2, 2020
- Posted
- July 29, 2020
- Recall Number
- D-1406-2020
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 35,928 bottles
- Firm Location
- Baltimore, MD, United States
Reason for Recall
Superpotent Drug: Out-of-specification (OOS) result observed in an assay test of retention samples.
Distribution
U.S.A. Nationwide
Lot / Code Info
Lot # F802189, Exp 10/2020, F900240, Exp 1/2021
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