Drugplain

tavaborole 43.5 mg/mL

tavaborole · SOLUTION · Mayne Pharma Commercial LLC

2 Recalls on Record
Plain English

tavaborole is a solution containing tavaborole at 43.5 mg/mL, taken topical. Manufactured by Mayne Pharma Commercial LLC.

Key Facts

Brand Name
tavaborole
Generic Name
tavaborole
NDC Code (Product)
51862-690
Manufacturer
Mayne Pharma Commercial LLC
Strength
43.5 mg/mL
Dosage Form
SOLUTION
Route
TOPICAL
Marketing Status
Application #
ANDA211297
Drug Class
Oxaborole Antifungal [EPC]
Marketing Start
02/01/2021

Recall History

2 Recalls on Record
Class II10/06/2025

VIONA PHARMACEUTICALS INC

Discoloration

OngoingVoluntary: Firm initiated
Class II08/12/2025

VIONA PHARMACEUTICALS INC

Discoloration

OngoingVoluntary: Firm initiated

Frequently Asked Questions

What is tavaborole used for?

tavaborole contains tavaborole. It is a solution taken topical. Consult your doctor for specific uses.

Is tavaborole a controlled substance?

tavaborole is not classified as a controlled substance by the DEA.

What is the generic name for tavaborole?

The generic name for tavaborole is tavaborole. There are 7 other brand versions of tavaborole.

What is the NDC code for tavaborole 43.5 mg/mL?

The NDC (National Drug Code) for tavaborole 43.5 mg/mL is 51862-690, listed by Mayne Pharma Commercial LLC.

Product NDC

51862-690

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)