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
- 68071-3357_3880e5dd-0433-2990-e063-6394a90a0ef8
- Product NDC
- 68071-3357
- Form
- TABLET, FILM COATED
- Composition / generic term
- Citalopram Hydrobromide
- Labeler
- NuCare Pharmaceuticals,Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20041028
- Source listing expiry
- 20261231
Source-listed ingredients
- CITALOPRAM HYDROBROMIDE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET, FILM COATED in 1 BOTTLE (68071-3357-1) · 68071-3357-1
- 30 TABLET, FILM COATED in 1 BOTTLE (68071-3357-3) · 68071-3357-3
- 40 TABLET, FILM COATED in 1 BOTTLE (68071-3357-4) · 68071-3357-4
- 45 TABLET, FILM COATED in 1 BOTTLE (68071-3357-5) · 68071-3357-5
- 60 TABLET, FILM COATED in 1 BOTTLE (68071-3357-6) · 68071-3357-6
- 90 TABLET, FILM COATED in 1 BOTTLE (68071-3357-9) · 68071-3357-9
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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