Corepharma LLC

FDA Regulatory Profile

Corepharma LLC appears in FDA public data with 1 recall, 0 510(k) clearances, 14 FDA inspections, and 1 compliance action on record. Its most recent recall (D-1079-2014, Class II) was initiated on December 13, 2013.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
14
Compliance Actions
1

Recent Recalls

NumberClassProductDate
D-1079-2014Class IIPyridostigmine Bromide Tablets USP, 60 mg, 100 count bottle, Rx only, Manufactured and Distributed bDecember 13, 2013