Data / Drug companies / Exeltis USA, Inc.
Exeltis USA, Inc.: 11 products in the FDA NDC directory, labeler code 0642
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Exeltis USA, Inc. (labeler code 0642) lists 11 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 11 prescription drugs. Its main marketing category is other unapproved drugs. The newest product started marketing on October 26, 2020.
The request: Watch Exeltis USA, Inc. (FDA labeler code 0642): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 0642
- Products in commercial distribution
- 11
- Packages
- 18
- Finished drugs by generic name
- 4
- Prescription products
- 11
- Over the counter products
- 0
- Flagged as original packager
- 11 of 11 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- May 4, 2001
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Other unapproved drugs | 6 | 54.5% |
| New drug applications (NDA) | 5 | 45.5% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 11 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Benznidazole | 2 | 1 |
| Drospirenone | 1 | 1 |
| Levonorgestrel and ethinyl estradiol | 1 | 19 |
| Metronidazole | 1 | 68 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Kit | 4 | 36.4% |
| Tablet | 3 | 27.3% |
| Capsule, liquid filled | 2 | 18.2% |
| Capsule, gelatin coated | 1 | 9.1% |
| Gel | 1 | 9.1% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Tyblume | 0642-7471 | Kit | New drug applications (NDA) | October 26, 2020 |
| Vitafol Fe Plus | 0642-7473 | Capsule, liquid filled | Other unapproved drugs | March 15, 2020 |
| Slynd | 0642-7470 | Kit | New drug applications (NDA) | June 6, 2019 |
| Benznidazole | 0642-7464 | Tablet | New drug applications (NDA) | March 30, 2018 |
| Benznidazole | 0642-7463 | Tablet | New drug applications (NDA) | March 30, 2018 |
| Nuvessa | 0642-7466 | Gel | New drug applications (NDA) | March 10, 2018 |
| Vitafol Ultra | 0642-0093 | Capsule, liquid filled | Other unapproved drugs | September 23, 2013 |
| Vitafol One | 0642-0070 | Capsule, gelatin coated | Other unapproved drugs | June 13, 2011 |
| Select-OB Plus DHA Prenatal Supplement Plus DHA | 0642-0075 | Kit | Other unapproved drugs | April 8, 2009 |
| Vitafol-OB Plus DHA Prenatal Supplement Plus DHA | 0642-0076 | Kit | Other unapproved drugs | February 16, 2007 |
| Strovite One Caplets | 0642-0207 | Tablet | Other unapproved drugs | May 4, 2001 |
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.