NDC 68645-520

Escitalopram Oxalate 20 mg tablet, film coated

On the label: Legacy Pharmaceutical Packaging. It's a repackaged product: Legacy Pharmaceutical Packaging rebottles it from Cipla USA., Inc.'s NDC 69097-849.

Where the pills inside were made

Raigad, India · makes it, tests it and packages it

Problems found, fixed voluntarily Last FDA inspection Apr 4, 2024. 7 inspections on record.

Hauppauge, NY, United States · makes it and tests it

No problems found Last FDA inspection Oct 25, 2023. 18 inspections on record.

Central Islip, NY, United States · tests it and packages it

Problems found, fixed voluntarily Last FDA inspection Jul 17, 2026. 4 inspections on record.

Generic drug: Escitalopram: see every company that makes it
Form: tablet, film coated, oral
Strength: 20 mg
Approval: ANDA ANDA078604
On the market since: Jun 16, 2016
Package NDCs: 68645-520-54
Official label: DailyMed (National Library of Medicine), updated Mar 11, 2026

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