Famotidine for Oral Suspension USP recall: CGMP Deviations
Famotidine for Oral Suspension USP, 40 mg/5 mL, 50 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202…
Why was Famotidine for Oral Suspension USP recalled?
CGMP Deviations
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: G606950, Exp 07/18
- Product
- Famotidine for Oral Suspension USP, 40 mg/5 mL, 50 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202…
- Recalling firm
- Lupin Pharmaceuticals Inc.
- Quantity
- 12,888 bottles
- Distribution
- Nationwide in the USA
- Recall date
- September 13, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)