DOPAMINE Drug Patent Profile
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Which patents cover Dopamine, and when can generic versions of Dopamine launch?
Dopamine is a drug marketed by Abbott, Abraxis Pharm, Am Regent, Baxter Hlthcare, Hikma Intl Pharms, Hospira, Igi Labs Inc, Intl Medication, Lyphomed, Smith And Nephew, Teligent, Teva Parenteral, Warner Chilcott, and B Braun. and is included in thirty-six NDAs.
The generic ingredient in DOPAMINE is dopamine hydrochloride. There are nine drug master file entries for this compound. Eight suppliers are listed for this compound. Additional details are available on the dopamine hydrochloride profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Dopamine
A generic version of DOPAMINE was approved as dopamine hydrochloride by HOSPIRA on February 4th, 1982.
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Summary for DOPAMINE
| US Patents: | 0 |
| Applicants: | 14 |
| NDAs: | 36 |
| Drug Prices: | Drug price information for DOPAMINE |
| DailyMed Link: | DOPAMINE at DailyMed |
US Patents and Regulatory Information for DOPAMINE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| B Braun | DOPAMINE HYDROCHLORIDE AND DEXTROSE 5% IN PLASTIC CONTAINER | dopamine hydrochloride | INJECTABLE;INJECTION | 019099-003 | Oct 15, 1986 | DISCN | Yes | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Teligent | DOPAMINE HYDROCHLORIDE | dopamine hydrochloride | INJECTABLE;INJECTION | 018656-001 | Jun 28, 1983 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Hospira | DOPAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER | dopamine hydrochloride | INJECTABLE;INJECTION | 018826-003 | Sep 30, 1983 | AP | RX | Yes | Yes | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Baxter Hlthcare | DOPAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER | dopamine hydrochloride | INJECTABLE;INJECTION | 019615-003 | Mar 27, 1987 | AP | RX | Yes | Yes | ⤷ 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 |
