Enalapril Maleate recall: Impurity Out of Spec
Enalapril Maleate, USP 5MG, 30-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0693-30
Why was Enalapril Maleate recalled?
Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.
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?
Lots: 51904-2, EXP: 01/31/2018; 51904-3, EXP: 02/28/2018; 51904-5, EXP: 03/31/2018; 52885-2, EXP: 03/31/2018, 53840-1, EXP: 5/28/2018.
- Product
- Enalapril Maleate, USP 5MG, 30-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0693-30
- Recalling firm
- Aidarex Pharmaceuticals LLC
- Quantity
- 25, 30-count bottles
- Distribution
- Distributed Nationwide in the USA
- Recall date
- August 1, 2018
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)