ZINC CHLORIDE IN PLASTIC CONTAINER Drug Patent Profile
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When do Zinc Chloride In Plastic Container patents expire, and what generic alternatives are available?
Zinc Chloride In Plastic Container is a drug marketed by Hospira and is included in one NDA.
The generic ingredient in ZINC CHLORIDE IN PLASTIC CONTAINER 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 In Plastic Container
A generic version of ZINC CHLORIDE IN PLASTIC CONTAINER was approved as zinc chloride by EXELA PHARMA on May 21st, 2021.
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Questions you can ask:
- What is the 5 year forecast for ZINC CHLORIDE IN PLASTIC CONTAINER?
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- What is Average Wholesale Price for ZINC CHLORIDE IN PLASTIC CONTAINER?
Summary for ZINC CHLORIDE IN PLASTIC CONTAINER
| US Patents: | 0 |
| Applicants: | 1 |
| NDAs: | 1 |
| Finished Product Suppliers / Packagers: | 1 |
| Raw Ingredient (Bulk) Api Vendors: | 160 |
| Clinical Trials: | 788 |
| Patent Applications: | 220 |
| DailyMed Link: | ZINC CHLORIDE IN PLASTIC CONTAINER at DailyMed |
Recent Clinical Trials for ZINC CHLORIDE IN PLASTIC CONTAINER
Identify potential brand extensions & 505(b)(2) entrants
| Sponsor | Phase |
|---|---|
| Insel Gruppe AG, University Hospital Bern | Phase 2 |
| Seoul National University Hospital | Phase 2 |
| University of Bern | Phase 2 |
Pharmacology for ZINC CHLORIDE IN PLASTIC CONTAINER
| Drug Class | Copper Absorption Inhibitor |
| Physiological Effect | Decreased Copper Ion Absorption |
US Patents and Regulatory Information for ZINC CHLORIDE IN PLASTIC CONTAINER
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
