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Last Updated: April 20, 2024

Ceftazidime - Generic Drug Details


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What are the generic drug sources for ceftazidime and what is the scope of freedom to operate?

Ceftazidime is the generic ingredient in ten branded drugs marketed by Acs Dobfar, Aurobindo Pharma Ltd, Wockhardt, B Braun, Glaxosmithkline, Pai Holdings Pharm, Hospira, Lilly, and Baxter Hlthcare, and is included in sixteen NDAs. Additional information is available in the individual branded drug profile pages.

There are seventeen drug master file entries for ceftazidime. Three suppliers are listed for this compound.

Summary for ceftazidime
Recent Clinical Trials for ceftazidime

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
Qianfoshan HospitalN/A
Arrevus Inc.Phase 2
King Faisal Specialist Hospital & Research CenterPhase 3

See all ceftazidime clinical trials

Pharmacology for ceftazidime
Medical Subject Heading (MeSH) Categories for ceftazidime

US Patents and Regulatory Information for ceftazidime

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Lilly TAZIDIME ceftazidime INJECTABLE;INJECTION 062655-002 Nov 20, 1985 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Glaxosmithkline PENTACEF ceftazidime INJECTABLE;INJECTION 064008-002 Mar 31, 1992 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Pai Holdings Pharm FORTAZ IN PLASTIC CONTAINER ceftazidime sodium INJECTABLE;INJECTION 050634-001 Apr 28, 1989 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Glaxosmithkline CEPTAZ ceftazidime INJECTABLE;INJECTION 050646-001 Sep 27, 1990 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Pai Holdings Pharm FORTAZ ceftazidime INJECTABLE;INJECTION 050578-003 Jul 19, 1985 DISCN Yes No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
B Braun CEFTAZIDIME IN DEXTROSE CONTAINER ceftazidime INJECTABLE;INJECTION 050823-002 Jun 13, 2011 DISCN Yes No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

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