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"70518-2067-0" National Drug Code (NDC)
Lamivudine 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2067-0)
(REMEDYREPACK INC.)
NDC Code
70518-2067-0
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2067-0)
Product NDC
70518-2067
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lamivudine
Non-Proprietary Name
Lamivudine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190508
Marketing Category Name
ANDA
Application Number
ANDA090457
Manufacturer
REMEDYREPACK INC.
Substance Name
LAMIVUDINE
Strength
150
Strength Unit
mg/1
Pharmacy Classes
Hepatitis 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]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2067-0