NDA (New Drug Application)
ANDA (Generic Application)
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It is formulated by 1 pharmaceutical company such as TETRAPHASE PHARMS. It is marketed under 1 brand name, including XERAVA. Available in 2 different strengths, such as EQ 50MG BASE/VIAL, EQ 100MG BASE/VIAL, and administered through 1 route including POWDER;INTRAVENOUS.
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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":"68577","ingredient":"ERAVACYCLINE DIHYDROCHLORIDE","trade_name":"XERAVA","family_id":"e652440819f64b129acf","publication_number":"US8796245B2","cleaned_patent_number":"8796245","drug_product_flag":"-","drug_substance_flag":"-","use_codes":["-"],"definitions":["-"],"patent_expire_date_text":"2029-08-07","publication_date":"2014-08-05","legal_status":"Granted"} | US8796245B2 | 05 Aug, 2014 | Granted | 07 Aug, 2029 | |
| {"application_id":"68638","ingredient":"ERAVACYCLINE DIHYDROCHLORIDE","trade_name":"XERAVA","family_id":"e652440819f64b129acf","publication_number":"US8906887B2","cleaned_patent_number":"8906887","drug_product_flag":"Y","drug_substance_flag":"-","use_codes":["-"],"definitions":["-"],"patent_expire_date_text":"2030-12-28","publication_date":"2014-12-09","legal_status":"Granted"} | US8906887B2 Formulation | 09 Dec, 2014 | Granted | 28 Dec, 2030 | |
| {"application_id":"68646","ingredient":"ERAVACYCLINE DIHYDROCHLORIDE","trade_name":"XERAVA","family_id":"9106baf2d96f43d68667","publication_number":"US10961190B2","cleaned_patent_number":"10961190","drug_product_flag":"-","drug_substance_flag":"Y","use_codes":["-"],"definitions":["-"],"patent_expire_date_text":"2037-10-19","publication_date":"2021-03-30","legal_status":"Granted"} | US10961190B2 Molecular | 30 Mar, 2021 | Granted | 19 Oct, 2037 | |
| {"application_id":"68654","ingredient":"ERAVACYCLINE DIHYDROCHLORIDE","trade_name":"XERAVA","family_id":"85e4cedd0052468aa8f3","publication_number":"US11578044B2","cleaned_patent_number":"11578044","drug_product_flag":"-","drug_substance_flag":"Y","use_codes":["-"],"definitions":["-"],"patent_expire_date_text":"2037-10-19","publication_date":"2023-02-14","legal_status":"Granted"} | US11578044B2 Molecular | 14 Feb, 2023 | Granted | 19 Oct, 2037 |
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.