"0173-0830-61" National Drug Code (NDC)

Levitra 1 BLISTER PACK in 1 CARTON (0173-0830-61) > 2 TABLET, FILM COATED in 1 BLISTER PACK
(GlaxoSmithKline LLC)

NDC Code0173-0830-61
Package Description1 BLISTER PACK in 1 CARTON (0173-0830-61) > 2 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC0173-0830
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLevitra
Non-Proprietary NameVardenafil Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20030825
End Marketing Date20211231
Marketing Category NameNDA
Application NumberNDA021400
ManufacturerGlaxoSmithKline LLC
Substance NameVARDENAFIL HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesPhosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]

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