NDC 50090-1577

Dicyclomine Hydrochloride 20 mg tablet

On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions 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
50090-1577-0 50090-1577-1 50090-1577-2 50090-1577-3 50090-1577-4 50090-1577-5 50090-1577-6 50090-1577-7 50090-1577-8
Official label
DailyMed (National Library of Medicine), updated Feb 9, 2024

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