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"51672-1326-8" National Drug Code (NDC)

Lustra 1 TUBE in 1 CARTON (51672-1326-8) > 3.5 g in 1 TUBE
(Taro Pharmaceuticals U.S.A., Inc.)

NDC Code51672-1326-8
Package Description1 TUBE in 1 CARTON (51672-1326-8) > 3.5 g in 1 TUBE
Product NDC51672-1326
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLustra
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/51672-1326-8





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