Composition
- Active ingredients
- CITALOPRAM HYDROBROMIDE EQ 10MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- CITALOPRAM HYDROBROMIDE EQ 40MG BASE · TabletNDA020822-003 · Prescription
- CITALOPRAM HYDROBROMIDE EQ 10MG BASE · TabletNDA020822-001 · Prescription
- CITALOPRAM HYDROBROMIDE EQ 60MG BASE · TabletNDA020822-004 · Discontinued
- CITALOPRAM HYDROBROMIDE EQ 20MG BASE · TabletNDA020822-002 · Prescription
- CITALOPRAM HYDROBROMIDE EQ 10MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · SolutionThis page
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA021046.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Celexa
- Active substance
- citalopram hydrobromide
- Route
- Oral
- Dosage form
- Solution
- Applicant
- Forest Labs
- Status
- Discontinued
- FDA approval
- 22 Dec 1999
- Application
- NDA021046-001