"67184-0521-1" National Drug Code (NDC)

Tenofovir Disoproxil Fumarate 30 TABLET, COATED in 1 BOTTLE, PLASTIC (67184-0521-1)
(Qilu Pharmaceutical Co., Ltd.)

NDC Code67184-0521-1
Package Description30 TABLET, COATED in 1 BOTTLE, PLASTIC (67184-0521-1)
Product NDC67184-0521
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTenofovir Disoproxil Fumarate
Non-Proprietary NameTenofovir Disoproxil Fumarate
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20200101
Marketing Category NameANDA
Application NumberANDA209498
ManufacturerQilu Pharmaceutical Co., Ltd.
Substance NameTENOFOVIR DISOPROXIL FUMARATE
Strength300
Strength Unitmg/1
Pharmacy ClassesHepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleosides [CS]

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