NDA (New Drug Application)
ANDA (Generic Application)
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It is formulated by 1 pharmaceutical company such as GLAXOSMITHKLINE. It is marketed under 1 brand name, including BLUJEPA. Available in 1 different strength, such as EQ 750MG BASE, and administered through 1 route including TABLET;ORAL.
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FDA approval history for this ingredient
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Key expiration dates for US patents covering this ingredient
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Latest drug strengths approved by FDA
| Strength | Route of Administration | Companies | Latest Approval Date |
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Patents approved by the FDA for the ingredient
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Patent Number | Publication Date | Legal Status | Patent Expiry Date | |
|---|---|---|---|---|---|
| {"application_id":"164473","ingredient":"GEPOTIDACIN MESYLATE","trade_name":"BLUJEPA","family_id":"","publication_number":"US8389524B2","cleaned_patent_number":"8389524","drug_product_flag":"Y","drug_substance_flag":"Y","use_codes":["-"],"definitions":["-"],"patent_expire_date_text":"2029-02-12","publication_date":"2013-03-05","legal_status":"Granted"} | US8389524B2 Molecular Formulation | 05 Mar, 2013 | Granted | 12 Feb, 2029 |
Country wise drug prices over the years
Country wise drug revenue over the years
Latest clinical trials and research studies for this ingredient
| NCT ID | Title | Status | Phase | Conditions | Start Date | Completion Date |
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Manufacturing Locations
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Note: Patent expirations and exclusivity timelines are dynamic and may shift based on litigation, regulatory extensions, and maintenance filings. Regular monitoring is advised.