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FDA Drug Approval, N018827, LOTRISONE
FDA Drug Approval, N018827, LOTRISONE
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NDA: 018827
Company: ORGANON
Drug Name: LOTRISONE
Active Ingredients: BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE
Strength: EQ 0.05% BASE;1%
Dosage Form/Route: CREAM;TOPICAL
Action Date: 07/10/1984
Marketing Status: Discontinued
Submission Classification: Type 4 - New Combination
Company: ORGANON
Drug Name: LOTRISONE
Active Ingredients: BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE
Strength: EQ 0.05% BASE;1%
Dosage Form/Route: CREAM;TOPICAL
Action Date: 07/10/1984
Marketing Status: Discontinued
Submission Classification: Type 4 - New Combination
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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