United States · FDA National Drug Code directory

Escitalopram

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 71610-425_09b866f0-4435-4d1a-9cc7-c6a5ea487cb0
Product NDC: 71610-425
Form: TABLET, FILM COATED
Composition / generic term: Escitalopram
Labeler: Aphena Pharma Solutions - Tennessee, LLC
Marketing category: ANDA
Marketing start / end (source format): 20130321
Source listing expiry: 20261231

Source-listed ingredients

ESCITALOPRAM OXALATE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

90 TABLET, FILM COATED in 1 BOTTLE (71610-425-60) · 71610-425-60

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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