FDA Drug Approval, N014602, CELESTONE SOLUSPAN

FDA Drug Approval, N014602, CELESTONE SOLUSPAN

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NDA: 014602
Company: ORGANON
Drug Name: CELESTONE SOLUSPAN
Active Ingredients: BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE
Strength: INJECTABLE;INJECTION
Dosage Form/Route: Prescription
Action Date: ORIG-1
Marketing Status: AB
Submission Classification: STANDARD

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