Data / Drug companies / Aucta Pharmaceuticals, Inc.
Aucta Pharmaceuticals, Inc.: 8 products in the FDA NDC directory, labeler code 73289
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Aucta Pharmaceuticals, Inc. (labeler code 73289) lists 8 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 8 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on April 9, 2026.
The request: Watch Aucta Pharmaceuticals, Inc. (FDA labeler code 73289): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 73289
- Products in commercial distribution
- 8
- Packages
- 11
- Finished drugs by generic name
- 5
- Prescription products
- 8
- Over the counter products
- 0
- Controlled substance products
- Schedule V 3
- Flagged as original packager
- 8 of 8 products that carry the flag
- Started marketing in the last 12 months
- 1
- Earliest marketing start
- May 5, 2023
- 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) | 5 | 62.5% |
| New drug applications (NDA) | 3 | 37.5% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 8 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Lacosamide | 3 | 57 |
| Sapropterin dihydrochloride | 2 | 10 |
| Arformoterol tartrate | 1 | 12 |
| Fosfomycin tromethamine | 1 | 9 |
| Deflazacort | 1 | 11 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule, extended release | 3 | 37.5% |
| Powder, for solution | 2 | 25% |
| Solution | 1 | 12.5% |
| Granule, for solution | 1 | 12.5% |
| Suspension | 1 | 12.5% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Fosfomycin Tromethamine | 73289-0067 | Granule, for solution | Generic drugs (ANDA) | April 9, 2026 |
| Pyquvi | 73289-0089 | Suspension | Generic drugs (ANDA) | June 30, 2025 |
| Zelvysia | 73289-0071 | Powder, for solution | Generic drugs (ANDA) | April 29, 2025 |
| Zelvysia | 73289-0070 | Powder, for solution | Generic drugs (ANDA) | April 29, 2025 |
| Arformoterol Tartrate Inhalation Solution | 73289-0072 | Solution | Generic drugs (ANDA) | February 11, 2025 |
| Motpoly xr | 73289-0065 | Capsule, extended release | New drug applications (NDA) | May 5, 2023 |
| Motpoly xr | 73289-0064 | Capsule, extended release | New drug applications (NDA) | May 5, 2023 |
| Motpoly xr | 73289-0063 | Capsule, extended release | New drug applications (NDA) | May 5, 2023 |
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.