"54838-566-70" National Drug Code (NDC)

NDC Code	54838-566-70
Package Description	240 mL in 1 BOTTLE, PLASTIC (54838-566-70)
Product NDC	54838-566
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lamivudine
Non-Proprietary Name	Lamivudine
Dosage Form	SOLUTION
Usage	ORAL
Start Marketing Date	20141031
End Marketing Date	20241130
Marketing Category Name	ANDA
Application Number	ANDA203564
Manufacturer	Lannett Company, Inc.
Substance Name	LAMIVUDINE
Strength	10
Strength Unit	mg/mL
Pharmacy Classes	Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Reverse Transcriptase Inhibitors [MoA]