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"48792-7890-2" National Drug Code (NDC)

Tadalafil 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (48792-7890-2)
(Sunshine Lake Pharma Co., Ltd.)

NDC Code48792-7890-2
Package Description60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (48792-7890-2)
Product NDC48792-7890
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTadalafil
Non-Proprietary NameTadalafil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190327
Marketing Category NameANDA
Application NumberANDA211335
ManufacturerSunshine Lake Pharma Co., Ltd.
Substance NameTADALAFIL
Strength20
Strength Unitmg/1
Pharmacy ClassesPhosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/48792-7890-2





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