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
- 69097-849_7e44336f-9692-42ff-af45-f98edd0c803c
- Product NDC
- 69097-849
- Form
- TABLET, FILM COATED
- Composition / generic term
- Escitalopram
- Labeler
- Cipla USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160616
- 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 (69097-849-02) · 69097-849-02
- 90 TABLET, FILM COATED in 1 BOTTLE (69097-849-05) · 69097-849-05
- 100 TABLET, FILM COATED in 1 BOTTLE (69097-849-07) · 69097-849-07
- 500 TABLET, FILM COATED in 1 BOTTLE (69097-849-12) · 69097-849-12
- 1000 TABLET, FILM COATED in 1 BOTTLE (69097-849-15) · 69097-849-15
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →