NDC 72934-4074

FINASTERIDE 0.1% / MINOXIDIL 5%

Finasteride 0.1% / Minoxidil 5%

FINASTERIDE 0.1% / MINOXIDIL 5% is a Topical Solution in the Human Prescription Drug category. It is labeled and distributed by Sincerus Florida, Llc. The primary component is Minoxidil; Finasteride.

• 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

Packaging

NDC 72934-4074-8

60 g in 1 BOTTLE, GLASS (72934-4074-8)

• Marketing Start Date: 2019-05-09
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72934-4074-8 [72934407408]

FINASTERIDE 0.1% / MINOXIDIL 5% SOLUTION

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-05-09

Drug Details

Active Ingredients

Ingredient	Strength
MINOXIDIL	5 g/100g

Pharmacological Class

• Arteriolar Vasodilation [PE]
• Arteriolar Vasodilator [EPC]
• 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]