NDC 70934-112

Escitalopram 10 mg tablet, film coated

On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's a repackaged product: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Accord Healthcare Inc.'s NDC 16729-169.

Where the pills inside were made

Intas Pharmaceuticals Limited

Ahmedabad, India · makes it and tests it

No problems found Last FDA inspection Jul 12, 2024. 10 inspections on record.

Intas Pharmaceuticals Limited

Ahmedabad, India · makes it and tests it

Serious problems, FDA action Last FDA inspection Dec 2, 2022. 7 inspections on record, 1 with serious problems.

Repackaging site

Product details

Generic drug
Escitalopram: see every company that makes it
Form
tablet, film coated
Strength
10 mg
Approval
ANDA ANDA202389
On the market since
May 9, 2018
Package NDCs
70934-112-30 70934-112-90
Official label
DailyMed (National Library of Medicine), updated Aug 3, 2021

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