Nicardipine Hydrochloride Injection recall: Subpotent
Nicardipine Hydrochloride Injection, 25 mg/10 ml (2.5 mg/mL),10 mL single dose vial, Rx only, Manufactured in India for: Mylan Institutional LLC…
Why was Nicardipine Hydrochloride Injection 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?
Lot #: UW301, UW302, Exp 02/15; UW303, UW304, UW305, UW306, Exp 04/15
- Product
- Nicardipine Hydrochloride Injection, 25 mg/10 ml (2.5 mg/mL),10 mL single dose vial, Rx only, Manufactured in India for: Mylan Institutional LLC…
- Recalling firm
- Mylan Institutional LLC
- Quantity
- 78,090 vials
- Distribution
- Nationwide
- Recall date
- March 25, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)