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
- 51672-1348_38e51a59-5806-77a6-e063-6394a90af6c6
- Product NDC
- 51672-1348
- Form
- SOLUTION
- Composition / generic term
- Escitalopram Oxalate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120503
- Source listing expiry
- 20261231
Source-listed ingredients
- ESCITALOPRAM OXALATE — 5 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (51672-1348-1) / 240 mL in 1 BOTTLE · 51672-1348-1
- 1 BOTTLE in 1 CARTON (51672-1348-8) / 120 mL in 1 BOTTLE · 51672-1348-8
- 1 BOTTLE in 1 CARTON (51672-1348-9) / 480 mL in 1 BOTTLE · 51672-1348-9
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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