"69097-167-02" National Drug Code (NDC)

Lamivudine 30 TABLET in 1 BOTTLE (69097-167-02)
(Cipla USA Inc.)

NDC Code69097-167-02
Package Description30 TABLET in 1 BOTTLE (69097-167-02)
Product NDC69097-167
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLamivudine
Non-Proprietary NameLamivudine
Dosage FormTABLET
UsageORAL
Start Marketing Date20170303
Marketing Category NameANDA
Application NumberANDA077221
ManufacturerCipla USA Inc.
Substance NameLAMIVUDINE
Strength300
Strength Unitmg/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]

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