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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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