NDA (New Drug Application)
ANDA (Generic Application)
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It is formulated by 3 pharmaceutical companies such as MSD SUB MERCK, ASPIRO, ZYDUS PHARMS. It is marketed under 2 brand names, including BRIDION, SUGAMMADEX SODIUM. Available in 2 different strengths, such as EQ 200MG BASE/2ML (EQ 100MG BASE/ML), EQ 500MG BASE/5ML (EQ 100MG BASE/ML), and administered through 1 route including SOLUTION;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":"73185","ingredient":"SUGAMMADEX SODIUM","trade_name":"BRIDION","family_id":"","publication_number":"USRE44733E1","cleaned_patent_number":"RE44733","drug_product_flag":"-, Y","drug_substance_flag":"-, Y","use_codes":["-"],"definitions":["-"],"patent_expire_date_text":"2026-07-27","publication_date":"2014-01-28","legal_status":"Granted"} | USRE44733E1 | 28 Jan, 2014 | Granted | 27 Jul, 2026 |
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.