Data / Drug companies / Ketamine hydrochloride
Ketamine hydrochloride: 11 companies and 28 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Ketamine hydrochloride is listed in the FDA National Drug Code Directory by 11 companies, with 28 products in commercial distribution. 24 of the products (85.7%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection; injection, solution; injection, solution, concentrate, and the newest product started marketing on September 8, 2026.
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- Companies listing it
- 11
- Products
- 28
- Generic (ANDA) products
- 24 (85.7%)
- Application numbers
- 7
- Controlled substance schedule
- Schedule III
- Routes
- Intramuscular, Intravenous
- Brand names
- Ketalar, Ketalar
- openFDA record search
- api.fda.gov
Companies that list ketamine hydrochloride
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Eugia US LLC | 4 | injection | Generic drugs (ANDA) | March 15, 2021 |
| Fresenius Kabi USA, LLC | 4 | injection | Generic drugs (ANDA) | July 10, 2023 |
| Gland Pharma Limited | 3 | injection, solution | Generic drugs (ANDA) | January 24, 2023 |
| Par Health USA, LLC | 3 | injection | New drug applications (NDA) | October 1, 2007 |
| Sagent Pharmaceuticals | 3 | injection, solution | Generic drugs (ANDA) | July 15, 2023 |
| Civica, Inc. | 2 | injection | Generic drugs (ANDA) | December 5, 2019 |
| Henry Schein, Inc. | 2 | injection | New drug applications (NDA) | September 8, 2026 |
| Hikma Pharmaceuticals USA Inc. | 2 | injection | Generic drugs (ANDA) | July 1, 1996 |
| Hospira, Inc. | 2 | injection, solution, concentrate | Generic drugs (ANDA) | November 30, 2004 |
| Medical Purchasing Solutions, LLC | 2 | injection; injection, solution, concentrate | Generic drugs (ANDA) | November 30, 2004 |
| Baxter Healthcare Corporation | 1 | injection | Generic drugs (ANDA) | September 17, 2025 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection | 19 | 67.9% |
| Injection, solution | 6 | 21.4% |
| Injection, solution, concentrate | 3 | 10.7% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 24 | 85.7% |
| New drug applications (NDA) | 4 | 14.3% |
Pharmacologic classes
| Class | Products |
|---|---|
| General Anesthetic | 28 |
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.