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
- 71335-2903_3cd3b722-6c0b-412f-ba74-6dc20f394e41
- Product NDC
- 71335-2903
- Form
- TABLET, FILM COATED
- Composition / generic term
- escitalopram
- 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
- 1000 TABLET, FILM COATED in 1 BOTTLE (71335-2903-1) · 71335-2903-1
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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