NDA (New Drug Application)
ANDA (Generic Application)
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It is formulated by 3 pharmaceutical companies such as FRESENIUS KABI USA, HIKMA, NIVAGEN PHARMS INC. It is marketed under 1 brand name, including REMIFENTANIL HYDROCHLORIDE. Available in 3 different strengths, such as EQ 1MG BASE/VIAL, EQ 2MG BASE/VIAL, EQ 5MG BASE/VIAL, and administered through 1 route including INJECTABLE;INJECTION.
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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
No US Orange Book patents found
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.