NDC 0527-1311

Terbutaline Sulfate 5 mg tablet

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
Terbutaline: every company that makes it
Form
tablet, oral
Strength
5 mg
Approval
ANDA ANDA077152
On the market since
Mar 25, 2005
Package NDCs
0527-1311-01 0527-1311-10
Official label
DailyMed (National Library of Medicine), updated Nov 12, 2020

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