NDC 0527-1367

Probenecid 500 mg tablet, film coated

On the label: Lannett Company, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Lannett Company, LLCSeymour, IN, United StatesMakes it, packages it and labels it Problems found, fixed voluntarilyOct 21, 2022 · 9 inspections, 1 with FDA action

Product details

Generic drug
Probenecid: every company that makes it
Form
tablet, film coated, oral
Strength
500 mg
Approval
ANDA ANDA080966
On the market since
Jul 29, 1976
Package NDCs
0527-1367-01 0527-1367-10
Official label
DailyMed (National Library of Medicine), updated Jan 5, 2021

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