NDA (New Drug Application)
ANDA (Generic Application)
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It is formulated by 1 pharmaceutical company such as BRISTOL. It is marketed under 1 brand name, including ZEPOSIA. Available in 3 different strengths, such as EQ 0.23MG BASE, EQ 0.46MG BASE, EQ 0.92MG BASE, and administered through 1 route including CAPSULE;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":"53888","ingredient":"OZANIMOD HYDROCHLORIDE","trade_name":"ZEPOSIA","family_id":"f70d52ab47774663ad01","publication_number":"US8796318B2","cleaned_patent_number":"8796318","drug_product_flag":"Y","drug_substance_flag":"Y","use_codes":["-"],"definitions":["-"],"patent_expire_date_text":"2029-05-14","publication_date":"2014-08-05","legal_status":"Granted"} | US8796318B2 Molecular Formulation | 05 Aug, 2014 | Granted | 14 May, 2029 | |
| {"application_id":"53889","ingredient":"OZANIMOD HYDROCHLORIDE","trade_name":"ZEPOSIA","family_id":"f70d52ab47774663ad01","publication_number":"US9382217B2","cleaned_patent_number":"9382217","drug_product_flag":"-","drug_substance_flag":"-","use_codes":["-"],"definitions":["-"],"patent_expire_date_text":"2029-05-14","publication_date":"2016-07-05","legal_status":"Granted"} | US9382217B2 | 05 Jul, 2016 | Granted | 14 May, 2029 | |
| {"application_id":"31938","ingredient":"OZANIMOD HYDROCHLORIDE","trade_name":"ZEPOSIA","family_id":"2f4533a017fc47d2b237","publication_number":"US10239846B2","cleaned_patent_number":"10239846","drug_product_flag":"-","drug_substance_flag":"-","use_codes":["-"],"definitions":["-"],"patent_expire_date_text":"2030-11-15","publication_date":"2019-03-26","legal_status":"Granted"} | US10239846B2 | 26 Mar, 2019 | Granted | 15 Nov, 2030 | |
| {"application_id":"53849","ingredient":"OZANIMOD HYDROCHLORIDE","trade_name":"ZEPOSIA","family_id":"f70d52ab47774663ad01","publication_number":"US8481573B2","cleaned_patent_number":"8481573","drug_product_flag":"Y","drug_substance_flag":"Y","use_codes":["-"],"definitions":["-"],"patent_expire_date_text":"2033-03-24","publication_date":"2013-07-09","legal_status":"Granted"} | US8481573B2 Molecular Formulation | 09 Jul, 2013 | Granted | 24 Mar, 2033 | |
| {"application_id":"37351","ingredient":"OZANIMOD HYDROCHLORIDE","trade_name":"ZEPOSIA","family_id":"b69da6ce8ef941e1a67a","publication_number":"US11680050B2","cleaned_patent_number":"11680050","drug_product_flag":"Y","drug_substance_flag":"Y","use_codes":["-"],"definitions":["-"],"patent_expire_date_text":"2038-09-30","publication_date":"2023-06-20","legal_status":"Granted"} | US11680050B2 Molecular Formulation | 20 Jun, 2023 | Granted | 30 Sep, 2038 |
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.