Nitrofurantoin Oral Suspension USP recall: Subpotent
Nitrofurantoin Oral Suspension USP, 25mg/5mL, 230 mL Bottle, Rx Only, Manufactured by: Novel Laboratories, Inc. Somerset, NJ 08873, Manufactured for…
Why was Nitrofurantoin Oral Suspension USP recalled?
Subpotent Drug and Failed Content Uniformity.
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#: S700065, Exp. 02/2019; 700619, Exp. 08/2019
- Product
- Nitrofurantoin Oral Suspension USP, 25mg/5mL, 230 mL Bottle, Rx Only, Manufactured by: Novel Laboratories, Inc. Somerset, NJ 08873, Manufactured for…
- Recalling firm
- LUPIN SOMERSET
- Quantity
- 3456 cartons
- Distribution
- Nationwide within the US
- Recall date
- July 18, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)