United States · FDA National Drug Code directory
Citalopram
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
- 65162-053_a42ab6f8-0664-4d9d-9da0-116bba7e55fc
- Product NDC
- 65162-053
- Form
- TABLET
- Composition / generic term
- Citalopram
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100406
- Source listing expiry
- 20261231
Source-listed ingredients
- CITALOPRAM HYDROBROMIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (65162-053-03) · 65162-053-03
- 100 TABLET in 1 BOTTLE (65162-053-10) · 65162-053-10
- 1000 TABLET in 1 BOTTLE (65162-053-11) · 65162-053-11
- 500 TABLET in 1 BOTTLE (65162-053-50) · 65162-053-50
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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