United States · FDA National Drug Code directory
escitalopram oxalate
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
- 71335-0322_dbb27d04-8711-4fa6-b0d3-de221b86775d
- Product NDC
- 71335-0322
- Form
- TABLET, FILM COATED
- Composition / generic term
- escitalopram oxalate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120911
- Source listing expiry
- 20271231
Source-listed ingredients
- ESCITALOPRAM OXALATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-0322-1) · 71335-0322-1
- 28 TABLET, FILM COATED in 1 BOTTLE (71335-0322-2) · 71335-0322-2
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-0322-3) · 71335-0322-3
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-0322-4) · 71335-0322-4
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-0322-5) · 71335-0322-5
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-0322-6) · 71335-0322-6
- 7 TABLET, FILM COATED in 1 BOTTLE (71335-0322-7) · 71335-0322-7
- 180 TABLET, FILM COATED in 1 BOTTLE (71335-0322-8) · 71335-0322-8
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-0322-9) · 71335-0322-9
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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