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"0173-0831-61" National Drug Code (NDC)

Levitra 1 BLISTER PACK in 1 CARTON (0173-0831-61) > 2 TABLET, FILM COATED in 1 BLISTER PACK
(GlaxoSmithKline LLC)

NDC Code0173-0831-61
Package Description1 BLISTER PACK in 1 CARTON (0173-0831-61) > 2 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC0173-0831
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLevitra
Non-Proprietary NameVardenafil Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20030825
End Marketing Date20211031
Marketing Category NameNDA
Application NumberNDA021400
ManufacturerGlaxoSmithKline LLC
Substance NameVARDENAFIL HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesPhosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0173-0831-61





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