"68788-6394-2" National Drug Code (NDC)

Lamivudine And Zidovudine 20 TABLET in 1 BOTTLE (68788-6394-2)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-6394-2
Package Description20 TABLET in 1 BOTTLE (68788-6394-2)
Product NDC68788-6394
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLamivudine And Zidovudine
Non-Proprietary NameLamivudine And Zidovudine
Dosage FormTABLET
UsageORAL
Start Marketing Date20160524
Marketing Category NameANDA
Application NumberANDA079128
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameLAMIVUDINE; ZIDOVUDINE
Strength150; 300
Strength Unitmg/1; mg/1
Pharmacy ClassesHepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]

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