"0093-7652-56" National Drug Code (NDC)

Vardenafil Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (0093-7652-56)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7652-56
Package Description30 TABLET, FILM COATED in 1 BOTTLE (0093-7652-56)
Product NDC0093-7652
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVardenafil Hydrochloride
Non-Proprietary NameVardenafil Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190103
Marketing Category NameANDA
Application NumberANDA091347
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameVARDENAFIL HYDROCHLORIDE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesPhosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]

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