Product NDC: | 0173-0663 |
Proprietary Name: | EPIVIR |
Non Proprietary Name: | lamivudine |
Active Ingredient(s): | 5 mg/mL & nbsp; lamivudine |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0173-0663 |
Labeler Name: | GlaxoSmithKline LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021004 |
Marketing Category: | NDA |
Start Marketing Date: | 19981223 |
Package NDC: | 0173-0663-00 |
Package Description: | 240 mL in 1 BOTTLE (0173-0663-00) |
NDC Code | 0173-0663-00 |
Proprietary Name | EPIVIR |
Package Description | 240 mL in 1 BOTTLE (0173-0663-00) |
Product NDC | 0173-0663 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | lamivudine |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 19981223 |
Marketing Category Name | NDA |
Labeler Name | GlaxoSmithKline LLC |
Substance Name | LAMIVUDINE |
Strength Number | 5 |
Strength Unit | mg/mL |
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] |