Drugplain

Tavaborole 43.5 mg/mL

Tavaborole · SOLUTION · Viona Pharmaceuticals Inc

No Recall History
Plain English

Tavaborole is a solution containing tavaborole at 43.5 mg/mL, taken topical. Manufactured by Viona Pharmaceuticals Inc.

Key Facts

Brand Name
Tavaborole
Generic Name
Tavaborole
NDC Code (Product)
72578-102
Manufacturer
Viona Pharmaceuticals Inc
Strength
43.5 mg/mL
Dosage Form
SOLUTION
Route
TOPICAL
Marketing Status
Application #
ANDA212294
Drug Class
Oxaborole Antifungal [EPC]
Marketing Start
04/24/2023

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective9 reports
off label use4 reports
cough3 reports
rash3 reports
accidental exposure to product2 reports
alopecia2 reports
asthma2 reports
death2 reports
dermatitis atopic2 reports
diarrhoea2 reports

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 2 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 72578-102, listed by Viona Pharmaceuticals Inc.

Product NDC

72578-102

Package NDC

72578-102-04

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

Data from openFDA · Public domain (CC0 1.0)