Drug recall D-1127-2017
Product
Famotidine for Oral Suspension USP, 40 mg/5 mL, 50 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Goa 403 722 INDIA, NDC 68180-150-01
Reason for recall
CGMP Deviations
Lots and codes
Lot #: G606950, Exp 07/18
Recall details
- Recalling firm
- Lupin Pharmaceuticals Inc., Baltimore, MD
- Quantity
- 12,888 bottles
- Distribution
- Nationwide in the USA
- Type
- Voluntary: Firm initiated
- Recall initiated
- May 2, 2017
- Terminated
- March 28, 2018
Related products
- Famotidine – drug information
- NDC 68180-150 Famotidine · Famotidine 40 mg/5mL · Lupin Pharmaceuticals, Inc.