| NDC Code | 72934-4069-8 |
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| Package Description | 60 g in 1 BOTTLE, GLASS (72934-4069-8) |
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| Product NDC | 72934-4069 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dexamethasone Sodium Phosphate 0.1% / Finasteride 0.1% / Minoxidil 5% |
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| Non-Proprietary Name | Dexamethasone Sodium Phosphate 0.1% / Finasteride 0.1% / Minoxidil 5% |
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| Dosage Form | SOLUTION |
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| Usage | TOPICAL |
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| Start Marketing Date | 20190509 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | Sincerus Florida, LLC |
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| Substance Name | MINOXIDIL; FINASTERIDE; DEXAMETHASONE SODIUM PHOSPHATE |
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| Strength | 5; .1; .1 |
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| Strength Unit | g/100g; g/100g; g/100g |
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| Pharmacy Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC],5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
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