Quinapril Tablets USP 5 mg recall: Impurity Out of Spec
Quinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD --- NDC 68180-556-09
Why was Quinapril Tablets USP 5 mg recalled?
Failed Impurities/Degradation Specifications; Impurity A
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?
Batch number G303703, exp 3/2016
- Product
- Quinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD --- NDC 68180-556-09
- Recalling firm
- Lupin Pharmaceuticals Inc.
- Quantity
- 15,168 bottes
- Distribution
- Nationwide
- Recall date
- April 12, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)