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"48792-7912-1" National Drug Code (NDC)

Sildenafil 30 TABLET, FILM COATED in 1 BOTTLE (48792-7912-1)
(Sunshine Lake Pharma Co., Ltd)

NDC Code48792-7912-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (48792-7912-1)
Product NDC48792-7912
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSildenafil
Non-Proprietary NameSildenafil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200611
Marketing Category NameANDA
Application NumberANDA213032
ManufacturerSunshine Lake Pharma Co., Ltd
Substance NameSILDENAFIL CITRATE
Strength50
Strength Unitmg/1
Pharmacy ClassesPhosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/48792-7912-1





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