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Epivir
Epivir - 49349-676-02 - (Lamivudine)
Drug Information of Epivir
| 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) |
Labeler Information of Epivir
| 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 Information of Epivir
| Package NDC: | 49349-676-02 |
| Package Description: | 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-676-02) |
NDC Information of Epivir
| NDC Code | 49349-676-02 |
| Proprietary Name | Epivir |
| Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-676-02) |
| 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] |
