OMEPRAZOLE AND CLARITHROMYCIN AND AMOXICILLIN Drug Patent Profile
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Which patents cover Omeprazole And Clarithromycin And Amoxicillin, and what generic alternatives are available?
Omeprazole And Clarithromycin And Amoxicillin is a drug marketed by Cumberland and is included in one NDA.
The generic ingredient in OMEPRAZOLE AND CLARITHROMYCIN AND AMOXICILLIN is amoxicillin; clarithromycin; omeprazole. There are forty-six drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the amoxicillin; clarithromycin; omeprazole profile page.
Summary for OMEPRAZOLE AND CLARITHROMYCIN AND AMOXICILLIN
US Patents: | 0 |
Applicants: | 1 |
NDAs: | 1 |
Finished Product Suppliers / Packagers: | 1 |
Clinical Trials: | 35 |
Formulation / Manufacturing: | see details |
DailyMed Link: | OMEPRAZOLE AND CLARITHROMYCIN AND AMOXICILLIN at DailyMed |
Recent Clinical Trials for OMEPRAZOLE AND CLARITHROMYCIN AND AMOXICILLIN
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
Pontificia Universidad Catolica de Chile | Phase 4 |
Hospital Universitário Oswaldo Cruz | Phase 2/Phase 3 |
Infan Industria Quimica Farmaceutica Nacional | Phase 2/Phase 3 |
See all OMEPRAZOLE AND CLARITHROMYCIN AND AMOXICILLIN clinical trials
Anatomical Therapeutic Chemical (ATC) Classes for OMEPRAZOLE AND CLARITHROMYCIN AND AMOXICILLIN
US Patents and Regulatory Information for OMEPRAZOLE AND CLARITHROMYCIN AND AMOXICILLIN
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cumberland | OMEPRAZOLE AND CLARITHROMYCIN AND AMOXICILLIN | amoxicillin; clarithromycin; omeprazole | CAPSULE, TABLET, CAPSULE, DELAYED RELEASE;ORAL | 050824-001 | Feb 8, 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 |