CUPRIC CHLORIDE Drug Patent Profile
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Which patents cover Cupric Chloride, and what generic alternatives are available?
Cupric Chloride is a drug marketed by Exela Pharma, Rk Pharma, Somerset, and Hospira. and is included in four NDAs.
The generic ingredient in CUPRIC CHLORIDE is cupric chloride. Five suppliers are listed for this compound. Additional details are available on the cupric chloride profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Cupric Chloride
A generic version of CUPRIC CHLORIDE was approved as cupric chloride by EXELA PHARMA on October 31st, 2022.
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Questions you can ask:
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Summary for CUPRIC CHLORIDE
| US Patents: | 0 |
| Applicants: | 4 |
| NDAs: | 4 |
| Finished Product Suppliers / Packagers: | 4 |
| Raw Ingredient (Bulk) Api Vendors: | 52 |
| Patent Applications: | 1,376 |
| DailyMed Link: | CUPRIC CHLORIDE at DailyMed |
US Patents and Regulatory Information for CUPRIC CHLORIDE
CUPRIC CHLORIDE is protected by zero US patents and one FDA Regulatory Exclusivity.
FDA Regulatory Exclusivity protecting CUPRIC CHLORIDE
COMPETITIVE GENERIC THERAPY
Exclusivity Expiration: ⤷ Sign Up
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Exela Pharma | CUPRIC CHLORIDE | cupric chloride | INJECTABLE;INJECTION | 212071-001 | Oct 31, 2022 | AP | RX | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | |||
| Hospira | CUPRIC CHLORIDE IN PLASTIC CONTAINER | cupric chloride | INJECTABLE;INJECTION | 018960-001 | Jun 26, 1986 | AP | RX | Yes | Yes | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | |||
| Rk Pharma | CUPRIC CHLORIDE | cupric chloride | INJECTABLE;INJECTION | 217626-001 | Apr 30, 2024 | AP | RX | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | |||
| Somerset | CUPRIC CHLORIDE | cupric chloride | INJECTABLE;INJECTION | 216113-001 | Apr 30, 2024 | AP | RX | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | |||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |
