"70518-2151-1" National Drug Code (NDC)

Tenofovir Disoproxil Fumarate 4 TABLET, FILM COATED in 1 BLISTER PACK (70518-2151-1)
(REMEDYREPACK INC.)

NDC Code70518-2151-1
Package Description4 TABLET, FILM COATED in 1 BLISTER PACK (70518-2151-1)
Product NDC70518-2151
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTenofovir Disoproxil Fumarate
Non-Proprietary NameTenofovir Disoproxil Fumarate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190624
Marketing Category NameANDA
Application NumberANDA090636
ManufacturerREMEDYREPACK INC.
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2151-1