www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"51672-1327-3" National Drug Code (NDC)

Lustra-af 1 TUBE in 1 CARTON (51672-1327-3) > 56.8 g in 1 TUBE
(Taro Pharmaceuticals U.S.A., Inc.)

NDC Code51672-1327-3
Package Description1 TUBE in 1 CARTON (51672-1327-3) > 56.8 g in 1 TUBE
Product NDC51672-1327
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLustra-af
Non-Proprietary NameHydroquinone
Dosage FormCREAM
UsageTOPICAL
Start Marketing Date20050120
Marketing Category NameUNAPPROVED DRUG OTHER
ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Substance NameHYDROQUINONE
Strength40
Strength Unitmg/g
Pharmacy ClassesMelanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA],Depigmenting Activity [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51672-1327-3





Copyright © 2007-2024 www.ndcvalidator.com