NDC 63629-8704

Tavaborole

Tavaborole

Tavaborole is a Topical Solution in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Tavaborole.

Product ID63629-8704_1ed32bb5-840c-46e6-9d23-327cf9f6d075
NDC63629-8704
Product TypeHuman Prescription Drug
Proprietary NameTavaborole
Generic NameTavaborole
Dosage FormSolution
Route of AdministrationTOPICAL
Marketing Start Date2021-01-10
Marketing CategoryANDA /
Application NumberANDA211848
Labeler NameBryant Ranch Prepack
Substance NameTAVABOROLE
Active Ingredient Strength44 mg/mL
Pharm ClassesBoron Compounds [CS], Oxaborole Antifungal [EPC], Protein Synthesis Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63629-8704-1

1 BOTTLE, GLASS in 1 CARTON (63629-8704-1) > 10 mL in 1 BOTTLE, GLASS
Marketing Start Date2021-01-10
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Tavaborole" or generic name "Tavaborole"

NDCBrand NameGeneric Name
0574-0157TavaboroleTavaborole
21922-020TavaboroleTAVABOROLE topical solution, 5%
51672-1397TAVABOROLETAVABOROLE
51862-690tavaboroletavaborole
62332-467TavaboroleTavaborole
63629-8704TavaboroleTavaborole
68180-958TavaboroleTavaborole
69097-686TAVABOROLETAVABOROLE
69238-1657TavaboroleTavaborole
71589-010TAVABOROLETAVABOROLE
72763-201TavaboroleTavaborole
10337-905KerydinTavaborole

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.