NDA (New Drug Application)
ANDA (Generic Application)
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It is formulated by 1 pharmaceutical company such as MEDICURE. It is marketed under 1 brand name, including ZYPITAMAG. Available in 3 different strengths, such as EQ 1MG BASE, EQ 2MG BASE, EQ 4MG 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":"104281","ingredient":"PITAVASTATIN MAGNESIUM","trade_name":"ZYPITAMAG","family_id":"7ec84421a1e14b6782fe","publication_number":"US8829186B2","cleaned_patent_number":"8829186","drug_product_flag":"Y","drug_substance_flag":"Y","use_codes":["-"],"definitions":["-"],"patent_expire_date_text":"2031-01-19","publication_date":"2014-09-09","legal_status":"Granted"} | US8829186B2 Molecular Formulation | 09 Sep, 2014 | Granted | 19 Jan, 2031 |
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.