Key Takeaway

Gabapentin Oral Solution, 250 mg/5 mL, 5 mL per unit dose cup, four unit dose cups per tray, For Institutional Use Only, Rx only, Hi-Tech Pharmacal Co., Inc, Amityville, NY 11701, NDC Tray: 50383-311- by Akorn, Inc. was recalled on March 8, 2021. The hazard: Failed Impurities/Degradation Specifications; out of specification for unknown impurity observed during 6 month stability testing

FDA Drug Class II Terminated

Gabapentin Oral Solution, 250 mg/5 mL, 5 mL per unit dose cup, four unit dose cups per tray, For Institutional Use Only, Rx only, Hi-Tech Pharmacal Co., Inc, Amityville, NY 11701, NDC Tray: 50383-311-

Recalled: March 8, 2021 ~8,183 unit dose cups units affected D-0301-2021

Description

Gabapentin Oral Solution, 250 mg/5 mL, 5 mL per unit dose cup, four unit dose cups per tray, For Institutional Use Only, Rx only, Hi-Tech Pharmacal Co., Inc, Amityville, NY 11701, NDC Tray: 50383-311-07; NDC Unit Dose Cup 50383-311-07

Hazard / Reason

Failed Impurities/Degradation Specifications; out of specification for unknown impurity observed during 6 month stability testing

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

Gabapentin Oral Solution, 250 mg/5 mL, 5 mL per unit dose cup, four unit dose cups per tray, For Institutional Use Only, Rx only, Hi-Tech Pharmacal Co., Inc, Amityville, NY 11701, NDC Tray: 50383-311-

Drugs

Company Information

Akorn, Inc.

Lake Forest, IL, United States

View all 192 recalls by Akorn, Inc. →

Distribution

Nationwide USA

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