Strength
150 mg/1
Manufacturer
Aurobindo Pharma LimitedNDC
65862002560
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
8/20/2025
Active Ingredients
LAMIVUDINEApproval Type
Generic (ANDA)
FDA Application
ANDA077464On Market Since
11/21/2016
Pharmacological Classes
Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor
Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor
Nucleoside Reverse Transcriptase Inhibitors
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