Key Takeaway

Alprazolam Tablets, USP, 0.25 mg, 10x10 per carton, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 51079-788-20 by Mylan Institutional, Inc. (d.b.a. UDL Laboratories) was recalled on January 18, 2019. The hazard: Failed Impurities/Degradation Specifications: Elevated levels of a known impurity detected during 6-month RT stability interval.

FDA Drug Class II Terminated

Alprazolam Tablets, USP, 0.25 mg, 10x10 per carton, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 51079-788-20

Recalled: January 18, 2019 ~10,281 UD cartons units affected D-1013-2019

Description

Alprazolam Tablets, USP, 0.25 mg, 10x10 per carton, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 51079-788-20

Hazard / Reason

Failed Impurities/Degradation Specifications: Elevated levels of a known impurity detected during 6-month RT stability interval.

Class II: Product that may cause temporary or medically reversible health consequences.

Class II indicates the product may cause temporary or medically reversible health effects. The probability of serious harm is considered remote.

Products Affected

Alprazolam Tablets, USP, 0.25 mg, 10x10 per carton, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 51079-788-20

Drugs

Company Information

Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Rockford, IL, United States

View all 22 recalls by Mylan Institutional, Inc. (d.b.a. UDL Laboratories) →

Distribution

Nationwide USA and Puerto Rico

Related Recalls

Frequently Asked Questions

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Compare the model number, lot code, serial number, or date range listed in the recall notice with the information on your product's label or packaging. For vehicles, check your VIN at NHTSA.gov/Recalls.

What remedy is available for this recall?

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