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"0173-0829-13" National Drug Code (NDC)

Levitra 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0173-0829-13)
(GlaxoSmithKline LLC)

NDC Code0173-0829-13
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0173-0829-13)
Product NDC0173-0829
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLevitra
Non-Proprietary NameVardenafil Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20030423
Marketing Category NameNDA
Application NumberNDA021400
ManufacturerGlaxoSmithKline LLC
Substance NameVARDENAFIL HYDROCHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesPhosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0173-0829-13





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