Data / Drug companies / Citalopram hydrobromide
Citalopram hydrobromide: 19 companies and 47 products in the FDA NDC directory
Citalopram hydrobromide is listed in the FDA National Drug Code Directory by 19 companies, with 47 products in commercial distribution. 47 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet; solution, and the newest product started marketing on April 28, 2025.
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- Companies listing it
- 19
- Products
- 47
- Generic (ANDA) products
- 47 (100.0%)
- Application numbers
- 4
- Routes
- Oral
- Brand names
- Citalopram
- openFDA record search
- api.fda.gov
Companies that list citalopram hydrobromide
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| A-S Medication Solutions | 7 | tablet, film coated; tablet | Generic drugs (ANDA) | October 18, 2007 |
| NuCare Pharmaceuticals,Inc. | 7 | tablet; tablet, film coated | Generic drugs (ANDA) | October 18, 2007 |
| Aurobindo Pharma Limited | 4 | tablet, film coated; solution | Generic drugs (ANDA) | August 28, 2006 |
| Proficient Rx LP | 4 | tablet; tablet, film coated | Generic drugs (ANDA) | October 18, 2007 |
| NCS HealthCare of Ky, LLC DBA Vangard Labs | 3 | tablet, film coated | Generic drugs (ANDA) | October 28, 2004 |
| Northwind Health Company, LLC | 3 | tablet, film coated | Generic drugs (ANDA) | March 2, 2022 |
| Preferred Pharmaceuticals Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | January 4, 2016 |
| Quallent Pharmaceuticals Health LLC | 3 | tablet, film coated | Generic drugs (ANDA) | August 1, 2023 |
| Bryant Ranch Prepack | 2 | tablet | Generic drugs (ANDA) | October 18, 2007 |
| Remedyrepack Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | April 28, 2025 |
| Advanced Rx of Tennessee, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | April 6, 2023 |
| Aphena Pharma Solutions - Tennessee, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | October 28, 2004 |
| Atlantic Biologicals Corp. | 1 | solution | Generic drugs (ANDA) | May 31, 2019 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Generic drugs (ANDA) | October 28, 2004 |
| Camber Pharmaceuticals, Inc. | 1 | solution | Generic drugs (ANDA) | December 21, 2015 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | October 28, 2004 |
| Proficient Rx LP | 1 | tablet | Generic drugs (ANDA) | October 18, 2007 |
| QPharma, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | October 28, 2004 |
| Quality Care Products, LLC | 1 | tablet | Generic drugs (ANDA) | August 30, 2019 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 29 | 61.7% |
| Tablet | 15 | 31.9% |
| Solution | 3 | 6.4% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 47 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Serotonin Reuptake Inhibitor | 47 |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.