KETAMINE Drug Patent Profile
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Which patents cover Ketamine, and what generic alternatives are available?
Ketamine is a drug marketed by Caplin, Eugia Pharma, Fresenius Kabi Usa, Gland, Hikma, Hospira, and Baxter Hlthcare Corp. and is included in seven NDAs.
The generic ingredient in KETAMINE is ketamine hydrochloride. There are eight drug master file entries for this compound. Twelve suppliers are listed for this compound. Additional details are available on the ketamine hydrochloride profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Ketamine
A generic version of KETAMINE was approved as ketamine hydrochloride by HIKMA on March 22nd, 1996.
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Questions you can ask:
- What is the 5 year forecast for KETAMINE?
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Summary for KETAMINE
| US Patents: | 0 |
| Applicants: | 7 |
| NDAs: | 7 |
| Drug Prices: | Drug price information for KETAMINE |
| DailyMed Link: | KETAMINE at DailyMed |
US Patents and Regulatory Information for KETAMINE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Caplin | KETAMINE HYDROCHLORIDE | ketamine hydrochloride | INJECTABLE;INJECTION | 217858-001 | Aug 7, 2025 | AP | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Fresenius Kabi Usa | KETAMINE HYDROCHLORIDE | ketamine hydrochloride | INJECTABLE;INJECTION | 215808-003 | Apr 18, 2025 | AP | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Eugia Pharma | KETAMINE HYDROCHLORIDE | ketamine hydrochloride | INJECTABLE;INJECTION | 076092-003 | Oct 25, 2002 | AP | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Hikma | KETAMINE HYDROCHLORIDE | ketamine hydrochloride | INJECTABLE;INJECTION | 074524-002 | Mar 22, 1996 | AP | RX | No | Yes | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Gland | KETAMINE HYDROCHLORIDE | ketamine hydrochloride | INJECTABLE;INJECTION | 216809-001 | Jan 24, 2023 | AP | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |


