"52817-295-00" National Drug Code (NDC)

Sildenafil Citrate 1000 TABLET, FILM COATED in 1 BOTTLE (52817-295-00)
(TruPharma LLC)

NDC Code52817-295-00
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (52817-295-00)
Product NDC52817-295
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSildenafil Citrate
Non-Proprietary NameSildenafil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160801
Marketing Category NameANDA
Application NumberANDA204883
ManufacturerTruPharma LLC
Substance NameSILDENAFIL CITRATE
Strength20
Strength Unitmg/1
Pharmacy ClassesPhosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]

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