Product NDC: | 49349-676 |
Proprietary Name: | Epivir |
Non Proprietary Name: | Lamivudine |
Active Ingredient(s): | 150 mg/1 & nbsp; Lamivudine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49349-676 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020564 |
Marketing Category: | NDA |
Start Marketing Date: | 20110913 |
Package NDC: | 49349-676-60 |
Package Description: | 60 TABLET, FILM COATED in 1 CANISTER (49349-676-60) |
NDC Code | 49349-676-60 |
Proprietary Name | Epivir |
Package Description | 60 TABLET, FILM COATED in 1 CANISTER (49349-676-60) |
Product NDC | 49349-676 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lamivudine |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20110913 |
Marketing Category Name | NDA |
Labeler Name | REMEDYREPACK INC. |
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] |