NDA (New Drug Application)
ANDA (Generic Application)
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It is formulated by 13 pharmaceutical companies such as CHARTWELL MOLECULAR, AVET LIFESCIENCES, LANNETT CO INC and others. It is marketed under 2 brand names, including ONDANSETRON HYDROCHLORIDE, ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE. Available in 5 different strengths, such as EQ 2MG BASE/ML, EQ 4MG BASE/5ML, EQ 8MG BASE and others, and administered through 3 routes including INJECTABLE;INJECTION, SOLUTION;ORAL, 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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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.