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
- 13668-011_48423caf-4df2-4653-a8ed-b28462757ed3
- Product NDC
- 13668-011
- Form
- TABLET, FILM COATED
- Composition / generic term
- Citalopram
- Labeler
- Torrent Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20071018
- Source listing expiry
- 20271231
Source-listed ingredients
- CITALOPRAM HYDROBROMIDE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (13668-011-01) · 13668-011-01
- 500 TABLET, FILM COATED in 1 BOTTLE (13668-011-05) · 13668-011-05
- 2800 TABLET, FILM COATED in 1 BOTTLE (13668-011-08) · 13668-011-08
- 30 TABLET, FILM COATED in 1 BOTTLE (13668-011-30) · 13668-011-30
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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