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FDA Drug Approval, N011984, DECADRON
FDA Drug Approval, N011984, DECADRON
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NDA: 011984
Company: MERCK
Drug Name: DECADRON
Active Ingredients: DEXAMETHASONE SODIUM PHOSPHATE
Strength: EQ 0.1% PHOSPHATE
Dosage Form/Route: SOLUTION/DROPS;OPHTHALMIC, OTIC
Action Date: 09/02/1959
Marketing Status: Discontinued
Submission Classification: Type 3 - New Dosage Form
Company: MERCK
Drug Name: DECADRON
Active Ingredients: DEXAMETHASONE SODIUM PHOSPHATE
Strength: EQ 0.1% PHOSPHATE
Dosage Form/Route: SOLUTION/DROPS;OPHTHALMIC, OTIC
Action Date: 09/02/1959
Marketing Status: Discontinued
Submission Classification: Type 3 - New Dosage Form
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- 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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