"70771-1622-4" National Drug Code (NDC)

Emtricitabine And Tenofovir Disoproxil Fumarate 10 BLISTER PACK in 1 CARTON (70771-1622-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1622-2)
(Zydus Lifesciences Limited)

NDC Code70771-1622-4
Package Description10 BLISTER PACK in 1 CARTON (70771-1622-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1622-2)
Product NDC70771-1622
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameEmtricitabine And Tenofovir Disoproxil Fumarate
Non-Proprietary NameEmtricitabine And Tenofovir Disoproxil Fumarate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210701
Marketing Category NameANDA
Application NumberANDA212689
ManufacturerZydus Lifesciences Limited
Substance NameEMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE
Strength167; 250
Strength Unitmg/1; mg/1
Pharmacy ClassesHepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleosides [CS], Nucleosides [CS]

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