Data / Drug companies / Covis Pharma US, Inc
Covis Pharma US, Inc: 18 products in the FDA NDC directory, labeler code 70515
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Covis Pharma US, Inc (labeler code 70515) lists 18 products in the FDA National Drug Code Directory, covering 7 finished drugs by generic name. By type: 18 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on October 29, 2019.
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- Labeler code
- 70515
- Products in commercial distribution
- 18
- Packages
- 27
- Finished drugs by generic name
- 7
- Prescription products
- 18
- Over the counter products
- 0
- Flagged as original packager
- 18 of 18 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- July 1, 2015
- 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) | 18 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 18 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Tizanidine hydrochloride | 4 | 25 |
| Digoxin | 4 | 33 |
| Nisoldipine | 3 | 3 |
| Ciclesonide | 3 | 1 |
| Omeprazole magnesium | 2 | 21 |
| Aclidinium bromide and formoterol fumarate | 1 | 1 |
| Aclidinium bromide | 1 | 1 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, solution | 4 | 22.2% |
| Tablet, film coated, extended release | 3 | 16.7% |
| Capsule | 3 | 16.7% |
| Aerosol, metered | 2 | 11.1% |
| Granule, delayed release | 2 | 11.1% |
| Powder, metered | 2 | 11.1% |
| Tablet | 1 | 5.6% |
| Spray | 1 | 5.6% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Central alpha-2 Adrenergic Agonist | 4 |
| Cardiac Glycoside | 4 |
| Dihydropyridine Calcium Channel Blocker | 3 |
| Proton Pump Inhibitor | 2 |
| Anticholinergic | 2 |
| beta2-Adrenergic Agonist | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Lanoxin | 70515-263 | Injection, solution | New drug applications (NDA) | October 29, 2019 |
| Lanoxin | 70515-261 | Injection, solution | New drug applications (NDA) | October 29, 2019 |
| Duaklir pressair | 70515-001 | Powder, metered | New drug applications (NDA) | March 29, 2019 |
| Zanaflex | 70515-606 | Capsule | New drug applications (NDA) | August 1, 2018 |
| Zanaflex | 70515-604 | Capsule | New drug applications (NDA) | August 1, 2018 |
| Zanaflex | 70515-602 | Capsule | New drug applications (NDA) | August 1, 2018 |
| Zanaflex | 70515-594 | Tablet | New drug applications (NDA) | August 1, 2018 |
| Omnaris | 70515-701 | Spray | New drug applications (NDA) | April 23, 2018 |
| Alvesco | 70515-712 | Aerosol, metered | New drug applications (NDA) | March 26, 2018 |
| Alvesco | 70515-711 | Aerosol, metered | New drug applications (NDA) | March 26, 2018 |
| Lanoxin | 70515-262 | Injection, solution | New drug applications (NDA) | September 15, 2017 |
| Lanoxin | 70515-260 | Injection, solution | New drug applications (NDA) | September 15, 2017 |
| Prilosec | 70515-625 | Granule, delayed release | New drug applications (NDA) | August 25, 2017 |
| Prilosec | 70515-610 | Granule, delayed release | New drug applications (NDA) | August 25, 2017 |
| Sular | 70515-503 | Tablet, film coated, extended release | New drug applications (NDA) | February 3, 2017 |
| Sular | 70515-501 | Tablet, film coated, extended release | New drug applications (NDA) | February 3, 2017 |
| Sular | 70515-500 | Tablet, film coated, extended release | New drug applications (NDA) | February 3, 2017 |
| Tudorza Pressair | 70515-002 | Powder, metered | New drug applications (NDA) | July 1, 2015 |
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.