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
- 13668-137_aa1ecae7-8a57-434f-a72b-088335b1a42c
- Product NDC
- 13668-137
- Form
- TABLET, FILM COATED
- Composition / generic term
- escitalopram
- Labeler
- Torrent Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120911
- Source listing expiry
- 20271231
Source-listed ingredients
- ESCITALOPRAM OXALATE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (13668-137-01) · 13668-137-01
- 500 TABLET, FILM COATED in 1 BOTTLE (13668-137-05) · 13668-137-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (13668-137-10) · 13668-137-10
- 2000 TABLET, FILM COATED in 1 BOTTLE (13668-137-20) · 13668-137-20
- 30 TABLET, FILM COATED in 1 BOTTLE (13668-137-30) · 13668-137-30
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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