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"70518-1083-0" National Drug Code (NDC)
Lamivudine 30 TABLET in 1 BLISTER PACK (70518-1083-0)
(REMEDYREPACK INC.)
NDC Code
70518-1083-0
Package Description
30 TABLET in 1 BLISTER PACK (70518-1083-0)
Product NDC
70518-1083
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lamivudine
Non-Proprietary Name
Lamivudine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20180327
Marketing Category Name
ANDA
Application Number
ANDA206974
Manufacturer
REMEDYREPACK INC.
Substance Name
LAMIVUDINE
Strength
300
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/70518-1083-0