United States · FDA National Drug Code directory
Citalopram Hydrobromide
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
- 65862-074_7cecadcf-9da0-41e4-b9fd-0fe04572dcd8
- Product NDC
- 65862-074
- Form
- SOLUTION
- Composition / generic term
- Citalopram Hydrobromide
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20060828
- Source listing expiry
- 20261231
Source-listed ingredients
- CITALOPRAM HYDROBROMIDE — 10 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 240 mL in 1 BOTTLE (65862-074-24) · 65862-074-24
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 →