NDC 0527-1282

Dicyclomine Hydrochloride 20 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, tests it, packages it and labels it Problems found, fixed voluntarilyOct 21, 2022 · 9 inspections, 1 with FDA action

Product details

Generic drug
Dicyclomine: every company that makes it
Form
tablet, oral
Strength
20 mg
Approval
ANDA ANDA040230
On the market since
Feb 26, 1999
Package NDCs
0527-1282-01 0527-1282-05 0527-1282-10
Official label
DailyMed (National Library of Medicine), updated Jun 4, 2020

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