NDA (New Drug Application)
ANDA (Generic Application)
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It is formulated by 1 pharmaceutical company such as KEY THERAP. It is marketed under 1 brand name, including ZONTIVITY. Available in 1 different strength, such as EQ 2.08MG 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":"104201","ingredient":"VORAPAXAR SULFATE","trade_name":"ZONTIVITY","family_id":"f0aec2b57f5c412c942c","publication_number":"US7304078B2","cleaned_patent_number":"7304078","drug_product_flag":"Y","drug_substance_flag":"Y","use_codes":["-"],"definitions":["-"],"patent_expire_date_text":"2027-12-23","publication_date":"2007-12-04","legal_status":"Court proceedings terminated"} | US7304078B2 Molecular Formulation | 04 Dec, 2007 | Court proceedings terminated | 23 Dec, 2027 |
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.