Tavaborole 43.5 mg/mL
Tavaborole · SOLUTION · Alembic Pharmaceuticals Limited
No Recall History
Plain English
Tavaborole is a solution containing tavaborole at 43.5 mg/mL, taken topical. Manufactured by Alembic Pharmaceuticals Limited.
Key Facts
- Brand Name
- Tavaborole
- Generic Name
- Tavaborole
- NDC Code (Product)
46708-467- Manufacturer
- Alembic Pharmaceuticals Limited
- Strength
- 43.5 mg/mL
- Dosage Form
- SOLUTION
- Route
- TOPICAL
- Marketing Status
- Application #
- ANDA212188
- Drug Class
- Oxaborole Antifungal [EPC]
- Marketing Start
- 02/18/2025
Recall History
No Recall HistorySide 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 46708-467, listed by Alembic Pharmaceuticals Limited.