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EPZICOM
EPZICOM - 0173-0742-00 - (abacavir sulfate and lamivudine)
Drug Information of EPZICOM
| Product NDC: | 0173-0742 |
| Proprietary Name: | EPZICOM |
| Non Proprietary Name: | abacavir sulfate and lamivudine |
| Active Ingredient(s): | 600; 300 mg/1; mg/1 & nbsp; abacavir sulfate and lamivudine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EPZICOM
| Product NDC: | 0173-0742 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021652 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20040818 |
Package Information of EPZICOM
| Package NDC: | 0173-0742-00 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (0173-0742-00) |
NDC Information of EPZICOM
| NDC Code | 0173-0742-00 |
| Proprietary Name | EPZICOM |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0173-0742-00) |
| Product NDC | 0173-0742 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | abacavir sulfate and lamivudine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20040818 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | ABACAVIR SULFATE; LAMIVUDINE |
| Strength Number | 600; 300 |
| Strength Unit | mg/1; 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],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
