ZINC CHLORIDE Drug Patent Profile
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When do Zinc Chloride patents expire, and what generic alternatives are available?
Zinc Chloride is a drug marketed by Exela Pharma and Hospira and is included in two NDAs.
The generic ingredient in ZINC CHLORIDE is zinc chloride. There are thirty-eight drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the zinc chloride profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Zinc Chloride
A generic version of ZINC CHLORIDE was approved as zinc chloride by EXELA PHARMA on May 21st, 2021.
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Summary for ZINC CHLORIDE
US Patents: | 0 |
Applicants: | 2 |
NDAs: | 2 |
Finished Product Suppliers / Packagers: | 1 |
Raw Ingredient (Bulk) Api Vendors: | 160 |
Clinical Trials: | 788 |
Patent Applications: | 220 |
DailyMed Link: | ZINC CHLORIDE at DailyMed |
Recent Clinical Trials for ZINC CHLORIDE
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
University of Bern | Phase 2 |
Il-Yang Pharm. Co., Ltd. | Phase 2 |
Insel Gruppe AG, University Hospital Bern | Phase 2 |
Pharmacology for ZINC CHLORIDE
Drug Class | Copper Absorption Inhibitor |
Physiological Effect | Decreased Copper Ion Absorption |
Anatomical Therapeutic Chemical (ATC) Classes for ZINC CHLORIDE
US Patents and Regulatory Information for ZINC CHLORIDE
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Exela Pharma | ZINC CHLORIDE | zinc chloride | INJECTABLE;INJECTION | 212007-001 | May 21, 2021 | AP | RX | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | |||
Hospira | ZINC CHLORIDE IN PLASTIC CONTAINER | zinc chloride | INJECTABLE;INJECTION | 018959-001 | Jun 26, 1986 | AP | RX | Yes | Yes | ⤷ 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 |