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
- 65162-021_058fe58a-fa86-459a-b79a-ac337913bc7e
- Product NDC
- 65162-021
- Form
- TABLET, FILM COATED
- Composition / generic term
- Escitalopram Oxalate
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170517
- Source listing expiry
- 20261231
Source-listed ingredients
- ESCITALOPRAM OXALATE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (65162-021-03) · 65162-021-03
- 90 TABLET, FILM COATED in 1 BOTTLE (65162-021-09) · 65162-021-09
- 1000 TABLET, FILM COATED in 1 BOTTLE (65162-021-11) · 65162-021-11
- 500 TABLET, FILM COATED in 1 BOTTLE (65162-021-50) · 65162-021-50
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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