Data / Drug companies / Santarus, Inc.
Santarus, Inc.: 6 products in the FDA NDC directory, labeler code 68012
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Santarus, Inc. (labeler code 68012) lists 6 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 6 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on March 20, 2018.
The request: Watch Santarus, Inc. (FDA labeler code 68012): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 68012
- Products in commercial distribution
- 6
- Packages
- 7
- Finished drugs by generic name
- 3
- Prescription products
- 6
- Over the counter products
- 0
- Flagged as original packager
- 1 of 1 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- June 15, 2004
- 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) | 6 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 6 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Metformin hydrochloride | 3 | 79 |
| Omeprazole and sodium bicarbonate | 2 | 11 |
| Budesonide | 1 | 40 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated, extended release | 3 | 50% |
| Powder, for suspension | 2 | 33.3% |
| Tablet, extended release | 1 | 16.7% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Biguanide | 3 |
| Proton Pump Inhibitor | 2 |
| Corticosteroid | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Glumetza | 68012-004 | Tablet, film coated, extended release | New drug applications (NDA) | March 20, 2018 |
| Zegerid | 68012-054 | Powder, for suspension | New drug applications (NDA) | June 15, 2014 |
| Uceris | 68012-309 | Tablet, extended release | New drug applications (NDA) | January 14, 2013 |
| Glumetza | 68012-003 | Tablet, film coated, extended release | New drug applications (NDA) | June 17, 2008 |
| Glumetza | 68012-002 | Tablet, film coated, extended release | New drug applications (NDA) | August 1, 2006 |
| Zegerid | 68012-052 | Powder, for suspension | New drug applications (NDA) | June 15, 2004 |
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.