Data / Drug companies / Plerixafor
Plerixafor: 13 companies and 13 products in the FDA NDC directory
Plerixafor is listed in the FDA National Drug Code Directory by 13 companies, with 13 products in commercial distribution. 11 of the products (84.6%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection, solution; solution; injection, and the newest product started marketing on June 16, 2025.
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- Companies listing it
- 13
- Products
- 13
- Generic (ANDA) products
- 11 (84.6%)
- Application numbers
- 9
- Routes
- Subcutaneous
- Brand names
- Mozobil
- openFDA record search
- api.fda.gov
Companies that list plerixafor
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Amneal Pharmaceuticals LLC | 1 | injection, solution | Generic drugs (ANDA) | July 25, 2023 |
| Bryant Ranch Prepack | 1 | injection, solution | Generic drugs (ANDA) | July 25, 2023 |
| Camber Pharmaceuticals, Inc. | 1 | injection, solution | Generic drugs (ANDA) | June 16, 2025 |
| Dr. Reddy's Laboratories Inc. | 1 | solution | Generic drugs (ANDA) | November 6, 2023 |
| Eugia US LLC | 1 | solution | Generic drugs (ANDA) | July 24, 2023 |
| Fresenius Kabi USA, LLC | 1 | injection, solution | Authorized generics (NDA) | June 22, 2023 |
| Gland Pharma Limited | 1 | injection, solution | Generic drugs (ANDA) | May 3, 2024 |
| Meitheal Pharmaceuticals Inc. | 1 | solution | Generic drugs (ANDA) | July 24, 2023 |
| Novadoz Pharmaceuticals LLC | 1 | injection, solution | Generic drugs (ANDA) | July 25, 2023 |
| Sagent Pharmaceuticals | 1 | injection, solution | Generic drugs (ANDA) | August 1, 2024 |
| Sanofi-Aventis U.S. LLC | 1 | injection, solution | New drug applications (NDA) | September 1, 2013 |
| Zydus Lifesciences Limited | 1 | injection | Generic drugs (ANDA) | July 28, 2023 |
| Zydus Pharmaceuticals USA Inc. | 1 | injection | Generic drugs (ANDA) | July 28, 2023 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, solution | 8 | 61.5% |
| Solution | 3 | 23.1% |
| Injection | 2 | 15.4% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 11 | 84.6% |
| New drug applications (NDA) | 1 | 7.7% |
| Authorized generics (NDA) | 1 | 7.7% |
Pharmacologic classes
| Class | Products |
|---|---|
| Hematopoietic Stem Cell Mobilizer | 13 |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). 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.