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
- 43602-474_c891ea0b-ed9d-4e75-a529-2b8a651034d2
- Product NDC
- 43602-474
- Form
- TABLET
- Composition / generic term
- escitalopram
- Labeler
- Ascent Pharmaceuticals, Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250715
- Source listing expiry
- 20261231
Source-listed ingredients
- ESCITALOPRAM OXALATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (43602-474-10) · 43602-474-10
- 30 TABLET in 1 BOTTLE (43602-474-30) · 43602-474-30
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 →