Product NDC: | 0173-0470 |
Proprietary Name: | EPIVIR |
Non Proprietary Name: | lamivudine |
Active Ingredient(s): | 150 mg/1 & nbsp; lamivudine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0173-0470 |
Labeler Name: | GlaxoSmithKline LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020564 |
Marketing Category: | NDA |
Start Marketing Date: | 19951121 |
Package NDC: | 0173-0470-01 |
Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE (0173-0470-01) |
NDC Code | 0173-0470-01 |
Proprietary Name | EPIVIR |
Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (0173-0470-01) |
Product NDC | 0173-0470 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | lamivudine |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 19951121 |
Marketing Category Name | NDA |
Labeler Name | GlaxoSmithKline LLC |
Substance Name | LAMIVUDINE |
Strength Number | 150 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |