Data / Drug companies / Aprepitant
Aprepitant: 7 companies and 28 products in the FDA NDC directory
Aprepitant is listed in the FDA National Drug Code Directory by 7 companies, with 28 products in commercial distribution. 21 of the products (75.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule; kit; emulsion, and the newest product started marketing on October 20, 2026.
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- Companies listing it
- 7
- Products
- 28
- Generic (ANDA) products
- 21 (75.0%)
- Application numbers
- 7
- Routes
- Oral, Intravenous
- Brand names
- Emend, Aponvie, Cinvanti
- openFDA record search
- api.fda.gov
Companies that list aprepitant
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Merck Sharp & Dohme LLC | 5 | capsule; kit | New drug applications (NDA) | December 17, 2015 |
| Torrent Pharmaceuticals Limited | 5 | capsule; kit | Generic drugs (ANDA) | October 20, 2026 |
| BluePoint Laboratories | 4 | capsule; kit | Generic drugs (ANDA) | February 10, 2026 |
| Glenmark Pharmaceuticals Inc., USA | 4 | capsule; kit | Generic drugs (ANDA) | October 12, 2017 |
| Golden State Medical Supply, Inc. | 4 | capsule; kit | Generic drugs (ANDA) | October 21, 2020 |
| Sandoz Inc | 4 | capsule; kit | Generic drugs (ANDA) | December 27, 2016 |
| Heron Therapeutics, Inc. | 2 | emulsion; injection, emulsion | New drug applications (NDA) | March 6, 2023 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule | 19 | 67.9% |
| Kit | 6 | 21.4% |
| Emulsion | 1 | 3.6% |
| Powder, for suspension | 1 | 3.6% |
| Injection, emulsion | 1 | 3.6% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 21 | 75% |
| New drug applications (NDA) | 7 | 25% |
Pharmacologic classes
| Class | Products |
|---|---|
| Substance P/Neurokinin-1 Receptor Antagonist | 22 |
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.