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"61919-889-30" National Drug Code (NDC)

Tadalafil 30 TABLET, FILM COATED in 1 BOTTLE (61919-889-30)
(Direct_Rx)

NDC Code61919-889-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (61919-889-30)
Product NDC61919-889
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTadalafil
Non-Proprietary NameTadalafil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190613
Marketing Category NameANDA
Application NumberANDA209908
ManufacturerDirect_Rx
Substance NameTADALAFIL
Strength5
Strength Unitmg/1
Pharmacy ClassesPhosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-889-30





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