"71205-231-10" National Drug Code (NDC)

Sildenafil Citrate 10 TABLET, FILM COATED in 1 BOTTLE (71205-231-10)
(Proficient Rx LP)

NDC Code71205-231-10
Package Description10 TABLET, FILM COATED in 1 BOTTLE (71205-231-10)
Product NDC71205-231
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSildenafil Citrate
Non-Proprietary NameSildenafil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20171211
Marketing Category NameANDA
Application NumberANDA091448
ManufacturerProficient Rx LP
Substance NameSILDENAFIL CITRATE
Strength100
Strength Unitmg/1
Pharmacy ClassesPhosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]

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