NDC 68071-1906

Citalopram Hydrobromide 20 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Torrent Pharma, Inc.'s NDC 13668-010.

India: 3

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Piramal Pharma LimitedPithampur, IndiaMakes it, tests it and packages it No problems foundMay 19, 2023 · 8 inspections
Torrent Pharmaceuticals LimitedIndrad, IndiaMakes it Problems found, fixed voluntarilyJun 12, 2024 · 7 inspections, 2 with FDA action
Torrent Pharmaceuticals LimitedBharuch, IndiaMakes it, tests it and packages it No problems foundJan 23, 2026 · 5 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Citalopram: every company that makes it
Form
tablet, oral
Strength
20 mg
Approval
ANDA ANDA078216
On the market since
Oct 18, 2007
Package NDCs
68071-1906-3 68071-1906-6 68071-1906-9
Official label
DailyMed (National Library of Medicine), updated Jul 11, 2024

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