Data / Drug companies / Par Health USA, LLC
Par Health USA, LLC: 14 products in the FDA NDC directory, labeler code 10370
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Par Health USA, LLC (labeler code 10370) lists 14 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 14 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on July 24, 2026.
The request: Watch Par Health USA, LLC (FDA labeler code 10370): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 10370
- Products in commercial distribution
- 14
- Packages
- 18
- Finished drugs by generic name
- 5
- Prescription products
- 14
- Over the counter products
- 0
- Flagged as original packager
- 14 of 14 products that carry the flag
- Started marketing in the last 12 months
- 7
- Earliest marketing start
- October 24, 2012
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 14 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 14 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Topiramate | 4 | 56 |
| Lamotrigine | 4 | 51 |
| Sitagliptin and metformin hydrochloride | 3 | 8 |
| Fluvoxamine maleate | 2 | 16 |
| Tretinoin | 1 | 28 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated, extended release | 7 | 50% |
| Capsule, extended release | 6 | 42.9% |
| Capsule | 1 | 7.1% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Anti-epileptic Agent | 4 |
| Mood Stabilizer | 4 |
| Biguanide | 3 |
| Dipeptidyl Peptidase 4 Inhibitor | 3 |
| Serotonin Reuptake Inhibitor | 2 |
| Retinoid | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Sitagliptin and Metformin hydrochloride | 10370-351 | Tablet, film coated, extended release | Generic drugs (ANDA) | July 24, 2026 |
| Sitagliptin and Metformin hydrochloride | 10370-318 | Tablet, film coated, extended release | Generic drugs (ANDA) | July 24, 2026 |
| Sitagliptin and Metformin hydrochloride | 10370-317 | Tablet, film coated, extended release | Generic drugs (ANDA) | July 24, 2026 |
| Lamotrigine Extended-Release | 10370-334 | Tablet, film coated, extended release | Generic drugs (ANDA) | January 2, 2026 |
| Lamotrigine Extended-Release | 10370-256 | Tablet, film coated, extended release | Generic drugs (ANDA) | January 2, 2026 |
| Lamotrigine Extended-Release | 10370-208 | Tablet, film coated, extended release | Generic drugs (ANDA) | January 2, 2026 |
| Lamotrigine Extended-Release | 10370-207 | Tablet, film coated, extended release | Generic drugs (ANDA) | January 2, 2026 |
| Topiramate | 10370-366 | Capsule, extended release | Generic drugs (ANDA) | May 26, 2023 |
| Topiramate | 10370-367 | Capsule, extended release | Generic drugs (ANDA) | May 24, 2023 |
| Topiramate | 10370-365 | Capsule, extended release | Generic drugs (ANDA) | May 24, 2023 |
| Topiramate | 10370-368 | Capsule, extended release | Generic drugs (ANDA) | March 24, 2023 |
| Fluvoxamine Maleate | 10370-176 | Capsule, extended release | Generic drugs (ANDA) | March 13, 2013 |
| Fluvoxamine Maleate | 10370-175 | Capsule, extended release | Generic drugs (ANDA) | March 13, 2013 |
| Tretinoin | 10370-268 | Capsule | Generic drugs (ANDA) | October 24, 2012 |
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.