Penicillamine Tablets USP 250 mg recall: Failed Dissolution
Penicillamine Tablets USP 250 mg, 100-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 Manufactured by: Lupin…
Why was Penicillamine Tablets USP 250 mg recalled?
Failed Dissolution 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?
Lot # M200498, Exp. June 2024
- Product
- Penicillamine Tablets USP 250 mg, 100-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 Manufactured by: Lupin…
- Recalling firm
- Lupin Pharmaceuticals Inc.
- Quantity
- N/A
- Distribution
- Product was distributed to 3 wholesale/distributor accounts.
- Recall date
- December 20, 2023
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)