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"60687-362-21" National Drug Code (NDC)

Lamivudine 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-362-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-362-11)
(American Health Packaging)

NDC Code60687-362-21
Package Description30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-362-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-362-11)
Product NDC60687-362
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLamivudine
Non-Proprietary NameLamivudine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180420
End Marketing Date20230831
Marketing Category NameANDA
Application NumberANDA077464
ManufacturerAmerican Health Packaging
Substance NameLAMIVUDINE
Strength150
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/60687-362-21





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