Avet Pharmaceuticals, Inc.

FDA Regulatory Profile

Avet Pharmaceuticals, Inc. appears in FDA public data with 4 recalls — including 2 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-1104-2020, Class II) was initiated on March 26, 2020.

Summary

Total Recalls
4 (2 Class I)
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-1104-2020Class IILosartan Potassium Tablets USP 100 mg, supplied in a) 30 count (NDC 23155-646-03, b) 90 count (NDC 2March 26, 2020
D-1103-2020Class IILosartan Potassium Tablets USP 50 mg, a) 30 count (NDC 23155-645-03), b) 90 count (NDC 23155-645-09)March 26, 2020
D-1255-2020Class ITetracycline HCL Capsules, USP, 250 mg, 100-count Bottle, Rx Only, Manufactured for: Heritage PharmMarch 23, 2020
D-1254-2020Class ITetracycline HCL Capsules, USP, 500 mg, 100-count Bottle, Rx Only, Manufactured for: Heritage PharmMarch 23, 2020