Avkare Incorporated

FDA Regulatory Profile

Avkare Incorporated appears in FDA public data with 5 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-1174-2018, Class II) was initiated on July 18, 2018.

Summary

Total Recalls
5
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-1174-2018Class IIAvKARE Valsartan and Hydrochlorothiazide 160 mg/12.5 mg tablets, 90-count bottle, Rx Only, ManufactuJuly 18, 2018
D-1177-2018Class IIAvKARE Valsartan and Hydrochlorothiazide 320 mg/25 mg tablets 90-count bottle, Rx Only, ManufacturedJuly 18, 2018
D-1173-2018Class IIAvKARE Valsartan and Hydrochlorothiazide 80 mg/12.5 mg tablets, 90-count bottle, Rx Only, ManufacturJuly 18, 2018
D-1176-2018Class IIAvKARE Valsartan and Hydrochlorothiazide 320 mg/12.5 mg tablets, 90-count bottle, Rx Only, ManufactuJuly 18, 2018
D-1175-2018Class IIAvKARE Valsartan and Hydrochlorothiazide 160 mg/25 mg tablets, 90-count bottle, Rx Only, ManufactureJuly 18, 2018