Home / Recalls / Qualitest Pharmaceuticals / D-1605-2014

D-1605-2014 Class III Terminated

Recalled by Qualitest Pharmaceuticals — Huntsville, AL

Recall Details

Product Type: Drugs
Report Date: October 1, 2014
Initiation Date: September 11, 2014
Termination Date: January 27, 2016
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 159,913 tablets

Product Description

MethylPREDNISolone TABLETS, USP 4 mg, a) 100 count bottles (NDC 0603-4593-21) and b) 21 count blister pack (NDC 0603-4593-15), Rx only, Mfg for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811

Reason for Recall

Subpotent; 6 month stability time point

Distribution Pattern

Nationwide

Code Information

100 count: T147F13A, Exp. 05/2015; 21 count: S003M14, Exp. 05/2015

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D1151-2015 Class III — Disulfiram tablets, USP, 500 mg, 100-count bottles, Rx only, Manufactured for an (June 18, 2015)
D00432-2015 Class III — PROMETHAZINE VC WITH CODEINE SYRUP, EACH 5 ml contains: Codeine Phosphate 10 mg (March 25, 2015)
D-0411-2015 Class II — PROMETHAZINE DM SYRUP (Promethazine Hydrochloride, USP and Dextromethorphan Hydr (February 23, 2015)
D-0397-2015 Class II — AMLODIPINE BESYLATE TABLETS USP, 10 mg*, 1000 count bottles (NDC 0603-2110-32), (February 13, 2015)
D-0331-2015 Class III — ACETAMINOPHEN and CODEINE PHOSPHATE ORAL SOLUTION USP, 120 mg/12 mg per 5 mL, pa (December 22, 2014)
D-1572-2014 Class II — OXYCODONE and ACETAMINOPHEN, USP 10 mg/325 mg, CII, 100 TABLETS, Rx only, Manufa (August 27, 2014)
D-0038-2015 Class II — CHILDREN'S Q-PAP, Acetaminophen, ORAL SUSPENSION, CHERRY FLAVOR, Active ingredie (August 6, 2014)
D-0039-2015 Class II — CHILDREN'S Q-PAP, Acetaminophen, ORAL SUSPENSION, GRAPE FLAVOR, Active ingredien (August 6, 2014)