FDAFDA · Food and drugs·Recall number D-1127-2017
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
Published September 13, 2017 · Recall initiated: May 2, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
CGMP Deviations
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Brand
- FAMOTIDINE
- Manufacturer
- Lupin Pharmaceuticals Inc.
- Distributor
- Nationwide in the USA
- UPC
- 0368180150015
- Lot
- Lot #: G606950, Exp 07/18
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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