Data / Drug companies / Hisun Pharmaceuticals USA, Inc.
Hisun Pharmaceuticals USA, Inc.: 17 products in the FDA NDC directory, labeler code 42658
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Hisun Pharmaceuticals USA, Inc. (labeler code 42658) lists 17 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 17 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on October 16, 2026.
The request: Watch Hisun Pharmaceuticals USA, Inc. (FDA labeler code 42658): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 42658
- Products in commercial distribution
- 17
- Packages
- 26
- Finished drugs by generic name
- 9
- Prescription products
- 17
- Over the counter products
- 0
- Flagged as original packager
- 11 of 11 products that carry the flag
- Started marketing in the last 12 months
- 6
- Earliest marketing start
- April 15, 2017
- 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) | 17 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 17 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Cyclophosphamide for injection | 3 | 3 |
| Irbesartan | 3 | 27 |
| Daunorubicin hydrochloride | 3 | 3 |
| Cladribine | 2 | 7 |
| Micafungin | 2 | 6 |
| Fludarabine phosphate | 1 | 6 |
| Dactinomycin | 1 | 4 |
| Ticagrelor | 1 | 32 |
| Prednisolone | 1 | 7 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, solution | 6 | 35.3% |
| Injection, powder, for solution | 5 | 29.4% |
| Tablet, film coated | 4 | 23.5% |
| Injection, powder, lyophilized, for solution | 1 | 5.9% |
| Tablet | 1 | 5.9% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Cyclophosphamide | 42658-035 | Injection, powder, for solution | Generic drugs (ANDA) | October 16, 2026 |
| Cyclophosphamide | 42658-034 | Injection, powder, for solution | Generic drugs (ANDA) | October 16, 2026 |
| Cyclophosphamide | 42658-033 | Injection, powder, for solution | Generic drugs (ANDA) | October 16, 2026 |
| Fludarabine Phosphate | 42658-024 | Injection, solution | Generic drugs (ANDA) | September 1, 2026 |
| Micafungin | 42658-023 | Injection, powder, for solution | Generic drugs (ANDA) | April 1, 2026 |
| Micafungin | 42658-022 | Injection, powder, for solution | Generic drugs (ANDA) | April 1, 2026 |
| Ticagrelor | 42658-115 | Tablet, film coated | Generic drugs (ANDA) | May 1, 2025 |
| Prednisolone | 42658-160 | Tablet | Generic drugs (ANDA) | September 1, 2024 |
| Dactinomycin | 42658-008 | Injection, powder, lyophilized, for solution | Generic drugs (ANDA) | May 8, 2024 |
| Cladribine | 42658-010 | Injection, solution | Generic drugs (ANDA) | May 18, 2020 |
| Cladribine | 42658-010 | Injection, solution | Generic drugs (ANDA) | May 18, 2020 |
| Daunorubicin Hydrochloride | 42658-021 | Injection, solution | Generic drugs (ANDA) | January 20, 2020 |
| Daunorubicin Hydrochloride | 42658-021 | Injection, solution | Generic drugs (ANDA) | January 20, 2020 |
| Daunorubicin Hydrochloride | 42658-019 | Injection, solution | Generic drugs (ANDA) | January 20, 2020 |
| Irbesartan | 42658-123 | Tablet, film coated | Generic drugs (ANDA) | April 15, 2017 |
| Irbesartan | 42658-122 | Tablet, film coated | Generic drugs (ANDA) | April 15, 2017 |
| Irbesartan | 42658-121 | Tablet, film coated | Generic drugs (ANDA) | April 15, 2017 |
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.