Rifampin Capsules USP 300mg recall: Subpotent
Rifampin Capsules USP 300mg, 30-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States…
Why was Rifampin Capsules USP 300mg recalled?
Subpotent Drug and Failed Impurities/Degradation Specifications
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?
A200817 exp 1/2024
- Product
- Rifampin Capsules USP 300mg, 30-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States…
- Recalling firm
- Lupin Pharmaceuticals Inc.
- Quantity
- 165,60 bottles
- Distribution
- Product was distributed to 32 Wholesale/distributor accounts who further distributed the product to 156 distribution sites.
- Recall date
- February 7, 2024
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)