Data / Drug companies / Salix Pharmaceuticals, Inc.
Salix Pharmaceuticals, Inc.: 16 products in the FDA NDC directory, labeler code 65649
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Salix Pharmaceuticals, Inc. (labeler code 65649) lists 16 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 16 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on May 4, 2018.
The request: Watch Salix Pharmaceuticals, Inc. (FDA labeler code 65649): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 65649
- Products in commercial distribution
- 16
- Packages
- 30
- Finished drugs by generic name
- 9
- Prescription products
- 16
- Over the counter products
- 0
- Flagged as original packager
- 15 of 15 products that carry the flag
- Started marketing in the last 12 months
- 0
- Products with a marketing end date set
- 2
- Earliest marketing start
- February 15, 1962
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 11 | 68.8% |
| Generic drugs (ANDA) | 3 | 18.8% |
| Other unapproved drugs | 2 | 12.5% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 16 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Methylnaltrexone bromide | 3 | 1 |
| Rifaximin | 2 | 3 |
| Azathioprine | 2 | 19 |
| Hydrocortisone acetate | 2 | 35 |
| Hydrocortisone | 1 | 171 |
| Mesalamine | 1 | 41 |
| Chlorothiazide | 1 | 1 |
| Plecanatide | 1 | 1 |
| Budesonide | 1 | 40 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 6 | 37.5% |
| Suppository | 2 | 12.5% |
| Kit | 2 | 12.5% |
| Injection, solution | 2 | 12.5% |
| Cream | 1 | 6.2% |
| Capsule, extended release | 1 | 6.2% |
| Suspension | 1 | 6.2% |
| Aerosol, foam | 1 | 6.2% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Corticosteroid | 4 |
| Opioid Antagonist | 3 |
| Rifamycin Antibacterial | 2 |
| Purine Antimetabolite | 2 |
| Aminosalicylate | 1 |
| Thiazide Diuretic | 1 |
| Guanylate Cyclase-C Agonist | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Plenvu | 65649-400 | Kit | New drug applications (NDA) | May 4, 2018 |
| Trulance Immediate release | 65649-003 | Tablet | New drug applications (NDA) | February 21, 2017 |
| Uceris | 65649-651 | Aerosol, foam | New drug applications (NDA) | December 1, 2014 |
| Xifaxan | 65649-303 | Tablet | New drug applications (NDA) | May 1, 2010 |
| Apriso | 65649-103 | Capsule, extended release | New drug applications (NDA) | October 31, 2008 |
| Relistor | 65649-150 | Tablet | New drug applications (NDA) | August 1, 2008 |
| Relistor | 65649-552 | Injection, solution | New drug applications (NDA) | April 24, 2008 |
| Relistor | 65649-551 | Injection, solution | New drug applications (NDA) | April 24, 2008 |
| MoviPrep | 65649-201 | Kit | New drug applications (NDA) | October 1, 2006 |
| Xifaxan | 65649-301 | Tablet | New drug applications (NDA) | July 25, 2004 |
| Proctocort | 65649-511 | Suppository | Other unapproved drugs | June 1, 2004 |
| Anusol HC | 65649-411 | Suppository | Other unapproved drugs | June 1, 2004 |
| Azasan | 65649-241 | Tablet | Generic drugs (ANDA) | April 1, 2003 |
| Azasan | 65649-231 | Tablet | Generic drugs (ANDA) | April 1, 2003 |
| Anusol HC | 65649-401 | Cream | Generic drugs (ANDA) | June 6, 1984 |
| Diuril | 65649-311 | Suspension | New drug applications (NDA) | February 15, 1962 |
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.