NDC 72934-4075

FINASTERIDE 0.1% / MINOXIDIL 7%

Finasteride 0.1% / Minoxidil 7%

FINASTERIDE 0.1% / MINOXIDIL 7% is a Topical Solution in the Human Prescription Drug category. It is labeled and distributed by Sincerus Florida, Llc. The primary component is Finasteride; Minoxidil.

• Product ID: 72934-4075_8747ab73-38f8-0828-e053-2a95a90a99cd
• NDC: 72934-4075
• Product Type: Human Prescription Drug
• Proprietary Name: FINASTERIDE 0.1% / MINOXIDIL 7%
• Generic Name: Finasteride 0.1% / Minoxidil 7%
• Dosage Form: Solution
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-05-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Sincerus Florida, LLC
• Substance Name: FINASTERIDE; MINOXIDIL
• Active Ingredient Strength: 0 g/100g; g/100g
• Pharm Classes: 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA],Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 72934-4075-8

60 g in 1 BOTTLE, GLASS (72934-4075-8)

• Marketing Start Date: 2019-05-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72934-4075-8 [72934407508]

FINASTERIDE 0.1% / MINOXIDIL 7% SOLUTION

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 2019-05-01

Drug Details

Active Ingredients

Ingredient	Strength
FINASTERIDE	.1 g/100g

Pharmacological Class

• 5-alpha Reductase Inhibitor [EPC]
• 5-alpha Reductase Inhibitors [MoA]
• Arteriolar Vasodilation [PE]
• Arteriolar Vasodilator [EPC]
• 5-alpha Reductase Inhibitor [EPC]
• 5-alpha Reductase Inhibitors [MoA]
• Arteriolar Vasodilation [PE]
• Arteriolar Vasodilator [EPC]