United States · FDA National Drug Code directory

Celexa

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
0456-4040_7a584cdb-dfe3-4360-a36d-7e8b93d7d7db
Product NDC
0456-4040
Form
TABLET, FILM COATED
Composition / generic term
citalopram
Labeler
Allergan, Inc.
Marketing category
NDA
Marketing start / end (source format)
19980717
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 (0456-4040-01) · 0456-4040-01

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.

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