| Product NDC: | 21695-367 |
| 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: | 21695-367 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020564 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19951121 |
| Package NDC: | 21695-367-06 |
| Package Description: | 6 TABLET, FILM COATED in 1 BOTTLE (21695-367-06) |
| NDC Code | 21695-367-06 |
| Proprietary Name | EPIVIR |
| Package Description | 6 TABLET, FILM COATED in 1 BOTTLE (21695-367-06) |
| Product NDC | 21695-367 |
| 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 | Rebel Distributors Corp |
| 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] |