NDC 71610-209

Dicyclomine Hydrochloride 20 mg tablet

On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged: Aphena Pharma Solutions - Tennessee, Inc. rebottles it from Lannett Company, Inc.'s NDC 0527-1282.

United States: 1

Where the pills inside were 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

Repackaging site

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
71610-209-09
Official label
DailyMed (National Library of Medicine), updated Dec 20, 2018

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