Rifampin Capsules USP recall: Subpotent
Rifampin Capsules USP, 300mg, 30-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by…
Why was Rifampin Capsules USP recalled?
Subpotent Drug
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 #: A201064, Exp. Date March 2024
- Product
- Rifampin Capsules USP, 300mg, 30-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by…
- Recalling firm
- Lupin Pharmaceuticals Inc.
- Quantity
- 26,352 bottles
- Distribution
- Nationwide within the United States
- Recall date
- April 17, 2024
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)