"59762-0035-2" National Drug Code (NDC)

Sildenafil Citrate 100 TABLET, FILM COATED in 1 BOTTLE (59762-0035-2)
(Greenstone LLC)

NDC Code59762-0035-2
Package Description100 TABLET, FILM COATED in 1 BOTTLE (59762-0035-2)
Product NDC59762-0035
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSildenafil Citrate
Non-Proprietary NameSildenafil Citrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20171201
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA020895
ManufacturerGreenstone LLC
Substance NameSILDENAFIL CITRATE
Strength50
Strength Unitmg/1
Pharmacy ClassesPhosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]

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