NDC 70934-089

escitalopram oxalate 20 mg tablet

On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Torrent Pharma, Inc.'s NDC 13668-137.

India: 3

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Torrent Pharmaceuticals LimitedIndrad, IndiaMakes it Problems found, fixed voluntarilyJun 12, 2024 · 7 inspections, 2 with FDA action
Torrent Pharmaceuticals LimitedBharuch, IndiaMakes it No problems foundJan 23, 2026 · 5 inspections, 1 with FDA action
VKT Pharma Private LimitedSrikakulam, IndiaMakes it Problems found, fixed voluntarilyFeb 7, 2025 · 2 inspections

Repackaging site

Product details

Generic drug
Escitalopram: every company that makes it
Form
tablet
Strength
20 mg
Approval
ANDA ANDA090939
On the market since
Mar 21, 2018
Package NDCs
70934-089-30 70934-089-90
Official label
DailyMed (National Library of Medicine), updated Jan 12, 2021

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