Details for Patent: 9,283,197
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Which drugs does patent 9,283,197 protect, and when does it expire?
Patent 9,283,197 protects EPINEPHRINE and is included in one NDA.
Summary for Patent: 9,283,197
Title: | More potent and less toxic formulations of epinephrine and methods of medical use |
Abstract: | The present invention provides pharmaceutical formulations of levorotatory-epinephrine, l-epinephrine, more potent and less toxic than existing pharmaceutical formulations of epinephrine, along with methods of producing and using these pharmaceutical formulations of l-epinephrine. |
Inventor(s): | Taneja; Jugal K. (Tampa, FL) |
Assignee: | |
Application Number: | 14/460,845 |
Patent Litigation and PTAB cases: | See patent lawsuits and PTAB cases for patent 9,283,197 |
Patent Claim Types: see list of patent claims | Formulation; Compound; | More… ↓ |
Drugs Protected by US Patent 9,283,197
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Patented / Exclusive Use | Submissiondate |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Bpi Labs | EPINEPHRINE | epinephrine | SOLUTION;INTRAVENOUS, INTRAOCULAR, INTRAMUSCULAR, SUBCUTANEOUS | 205029-001 | Jul 29, 2014 | RX | Yes | Yes | ⤷ Subscribe | ⤷ Subscribe | Y | Y | EMERGENCY TREATMENT OF ALLERGIC REACTIONS (TYPE I), INCLUDING ANAPHYLAXIS | ⤷ Subscribe | ||
Bpi Labs | EPINEPHRINE | epinephrine | SOLUTION;INTRAVENOUS, INTRAOCULAR, INTRAMUSCULAR, SUBCUTANEOUS | 205029-001 | Jul 29, 2014 | RX | Yes | Yes | ⤷ Subscribe | ⤷ Subscribe | Y | Y | INCREASING MEAN ARTERIAL BLOOD PRESSURE IN ADULT PATIENTS WITH HYPOTENSION ASSOCIATED WITH SEPTIC SHOCK | ⤷ Subscribe | ||
Bpi Labs | EPINEPHRINE | epinephrine | SOLUTION;INTRAVENOUS, INTRAOCULAR, INTRAMUSCULAR, SUBCUTANEOUS | 205029-001 | Jul 29, 2014 | RX | Yes | Yes | ⤷ Subscribe | ⤷ Subscribe | Y | Y | INDUCTION AND MAINTENANCE OF MYDRIASIS DURING INTRAOCULAR SURGERY | ⤷ Subscribe | ||
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Patented / Exclusive Use | >Submissiondate |