"53002-1719-3" National Drug Code (NDC)

Sildenafil 30 TABLET, FILM COATED in 1 BOTTLE (53002-1719-3)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-1719-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (53002-1719-3)
Product NDC53002-1719
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSildenafil
Non-Proprietary NameSildenafil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130531
Marketing Category NameANDA
Application NumberANDA078380
ManufacturerRPK Pharmaceuticals, Inc.
Substance NameSILDENAFIL CITRATE
Strength20
Strength Unitmg/1
Pharmacy ClassesPhosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]

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