Data / Drug companies / Sandoz Inc
Sandoz Inc: 34 products in the FDA NDC directory, labeler code 66758
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Sandoz Inc (labeler code 66758) lists 34 products in the FDA National Drug Code Directory, covering 15 finished drugs by generic name. By type: 34 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on July 7, 2017.
The request: Watch Sandoz Inc (FDA labeler code 66758): each new product listing and each discontinued product. $10 of work on sign-up, no card.
SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.
- Labeler code
- 66758
- Products in commercial distribution
- 34
- Packages
- 46
- Finished drugs by generic name
- 15
- Prescription products
- 34
- Over the counter products
- 0
- Controlled substance products
- Schedule II 14
- Flagged as original packager
- 29 of 29 products that carry the flag
- Started marketing in the last 12 months
- 0
- Products with a marketing end date set
- 4
- Earliest marketing start
- December 31, 1955
- 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) | 34 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 34 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Patch, extended release | 8 | 23.5% |
| Capsule, extended release | 8 | 23.5% |
| Tablet | 6 | 17.6% |
| Injection, solution | 2 | 5.9% |
| Suspension/ drops | 2 | 5.9% |
| Capsule | 2 | 5.9% |
| Ointment | 2 | 5.9% |
| Emulsion | 1 | 2.9% |
| Tablet, extended release | 1 | 2.9% |
| Injection | 1 | 2.9% |
| Solution/ drops | 1 | 2.9% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Hycamtin | 66758-101 | Capsule | New drug applications (NDA) | July 7, 2017 |
| Hycamtin | 66758-102 | Capsule | New drug applications (NDA) | February 24, 2017 |
| Arranon | 66758-165 | Injection | New drug applications (NDA) | October 5, 2016 |
| Docetaxel | 66758-050 | Injection, solution | New drug applications (NDA) | June 29, 2011 |
| Durezol | 66758-086 | Emulsion | New drug applications (NDA) | January 25, 2011 |
| Exelon | 66758-144 | Patch, extended release | New drug applications (NDA) | July 6, 2007 |
| Exelon | 66758-143 | Patch, extended release | New drug applications (NDA) | July 6, 2007 |
| Exelon | 66758-142 | Patch, extended release | New drug applications (NDA) | July 6, 2007 |
| Reclast | 66758-155 | Injection, solution | New drug applications (NDA) | April 1, 2007 |
| Travatan Z | 66758-095 | Solution/ drops | New drug applications (NDA) | October 20, 2006 |
| Focalin XR | 66758-242 | Capsule, extended release | New drug applications (NDA) | May 31, 2005 |
| Focalin XR | 66758-241 | Capsule, extended release | New drug applications (NDA) | May 31, 2005 |
| Focalin XR | 66758-240 | Capsule, extended release | New drug applications (NDA) | May 31, 2005 |
| Focalin XR | 66758-239 | Capsule, extended release | New drug applications (NDA) | May 31, 2005 |
| Focalin XR | 66758-238 | Capsule, extended release | New drug applications (NDA) | May 31, 2005 |
| Focalin XR | 66758-237 | Capsule, extended release | New drug applications (NDA) | May 31, 2005 |
| Focalin XR | 66758-236 | Capsule, extended release | New drug applications (NDA) | May 31, 2005 |
| Focalin XR | 66758-235 | Capsule, extended release | New drug applications (NDA) | May 31, 2005 |
| Focalin | 66758-252 | Tablet | New drug applications (NDA) | November 30, 2001 |
| Focalin | 66758-251 | Tablet | New drug applications (NDA) | November 30, 2001 |
| Focalin | 66758-250 | Tablet | New drug applications (NDA) | November 30, 2001 |
| Lescol XL | 66758-211 | Tablet, extended release | New drug applications (NDA) | October 6, 2000 |
| Cipro hc | 66758-087 | Suspension/ drops | New drug applications (NDA) | March 15, 1999 |
| Vivelle-Dot | 66758-149 | Patch, extended release | New drug applications (NDA) | January 8, 1999 |
| Vivelle-Dot | 66758-148 | Patch, extended release | New drug applications (NDA) | January 8, 1999 |
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.