NDC 67296-0683

Citalopram 10 mg tablet, film coated

On the label: RedPharm Drug Inc.. It's repackaged: RedPharm Drug Inc. rebottles it from Aurolife Pharma LLC's NDC 13107-006.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Aurolife Pharma LLCDayton, NJ, United StatesMakes it Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action
Aurolife Pharma LLCDayton, NJ, United StatesPackages it, labels it, repackages it and relabels it Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action

Product details

Generic drug
Citalopram: every company that makes it
Form
tablet, film coated
Strength
10 mg
Approval
ANDA ANDA077031
On the market since
Oct 28, 2004
Package NDCs
67296-0683-1
Official label
DailyMed (National Library of Medicine), updated Aug 17, 2011

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