CEFTAZIDIME IN DEXTROSE CONTAINER Drug Patent Profile
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Which patents cover Ceftazidime In Dextrose Container, and when can generic versions of Ceftazidime In Dextrose Container launch?
Ceftazidime In Dextrose Container is a drug marketed by B Braun and is included in one NDA.
The generic ingredient in CEFTAZIDIME IN DEXTROSE CONTAINER is ceftazidime. There are seventeen drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the ceftazidime profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Ceftazidime In Dextrose Container
A generic version of CEFTAZIDIME IN DEXTROSE CONTAINER was approved as ceftazidime by ACS DOBFAR on November 20th, 1985.
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Questions you can ask:
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Summary for CEFTAZIDIME IN DEXTROSE CONTAINER
US Patents: | 0 |
Applicants: | 1 |
NDAs: | 1 |
Clinical Trials: | 68 |
Formulation / Manufacturing: | see details |
DailyMed Link: | CEFTAZIDIME IN DEXTROSE CONTAINER at DailyMed |
![CEFTAZIDIME IN DEXTROSE CONTAINER drug patent expirations Drug patent expirations by year for CEFTAZIDIME IN DEXTROSE CONTAINER](/p/graph/s/t/CEFTAZIDIME_IN_DEXTROSE_CONTAINER-patent-expirations.png)
Recent Clinical Trials for CEFTAZIDIME IN DEXTROSE CONTAINER
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
Tata Memorial Centre | Phase 2 |
Qianfoshan Hospital | N/A |
Arrevus Inc. | Phase 2 |
US Patents and Regulatory Information for CEFTAZIDIME IN DEXTROSE CONTAINER
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
B Braun | CEFTAZIDIME IN DEXTROSE CONTAINER | ceftazidime | INJECTABLE;INJECTION | 050823-001 | Jun 13, 2011 | DISCN | Yes | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
B Braun | CEFTAZIDIME IN DEXTROSE CONTAINER | ceftazidime | INJECTABLE;INJECTION | 050823-002 | Jun 13, 2011 | DISCN | Yes | 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 |