Product ID | 72934-4074_8861f646-2de1-e95c-e053-2a95a90a2041 |
NDC | 72934-4074 |
Product Type | Human Prescription Drug |
Proprietary Name | FINASTERIDE 0.1% / MINOXIDIL 5% |
Generic Name | Finasteride 0.1% / Minoxidil 5% |
Dosage Form | Solution |
Route of Administration | TOPICAL |
Marketing Start Date | 2019-05-09 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | Sincerus Florida, LLC |
Substance Name | MINOXIDIL; FINASTERIDE |
Active Ingredient Strength | 5 g/100g; g/100g |
Pharm Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC],5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |