AptaPharma Inc.

FDA Regulatory Profile

AptaPharma Inc. appears in FDA public data with 1 recall, 0 510(k) clearances, 5 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-0787-2022, Class III) was initiated on March 29, 2022.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
5
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-0787-2022Class IIIWal-Tussin DM (dextromethorphan HBr/Guaifenesin), 12 FL OZ (354 mL) bottles, Distributed By: WalgreeMarch 29, 2022