FDA recall D-0998-2020

Mayne Pharma Inc · Class II · drug

Product

Carbidopa and Levodopa Tablets, USP 25 mg/250mg, 100 ct bottle, Rx Only, Mayne Pharma, Greenville, NC 27834. NDC 51862-858-01

Reason for recall

Product Mix-Up: A foreign tablet was found in bottle.

Distribution

Distributed Nationwide in the USA

Key facts

Status
Terminated
Initiation date
2020-03-02
Report date
2020-03-18
Termination date
2021-10-28
Voluntary/Mandated
Voluntary: Firm initiated
Location
Greenville, NC, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0998-2020