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FDA Drug Approval, N019698, TORADOL
FDA Drug Approval, N019698, TORADOL
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NDA: 019698
Company: ROCHE PALO
Drug Name: TORADOL
Active Ingredients: KETOROLAC TROMETHAMINE
Strength: 30MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 11/30/1989
Marketing Status: Discontinued
Submission Classification: Type 1 - New Molecular Entity
Company: ROCHE PALO
Drug Name: TORADOL
Active Ingredients: KETOROLAC TROMETHAMINE
Strength: 30MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 11/30/1989
Marketing Status: Discontinued
Submission Classification: Type 1 - New Molecular Entity
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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