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COMBIVIR
COMBIVIR - 49702-202-29 - (lamivudine and zidovudine)
Drug Information of COMBIVIR
| Product NDC: | 49702-202 |
| Proprietary Name: | COMBIVIR |
| Non Proprietary Name: | lamivudine and zidovudine |
| Active Ingredient(s): | 150; 300 mg/1; mg/1 & nbsp; lamivudine and zidovudine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of COMBIVIR
| Product NDC: | 49702-202 |
| Labeler Name: | ViiV Healthcare Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020857 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101019 |
Package Information of COMBIVIR
| Package NDC: | 49702-202-29 |
| Package Description: | 120 TABLET, FILM COATED in 1 DOSE PACK (49702-202-29) |
NDC Information of COMBIVIR
| NDC Code | 49702-202-29 |
| Proprietary Name | COMBIVIR |
| Package Description | 120 TABLET, FILM COATED in 1 DOSE PACK (49702-202-29) |
| Product NDC | 49702-202 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lamivudine and zidovudine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20101019 |
| Marketing Category Name | NDA |
| Labeler Name | ViiV Healthcare Company |
| Substance Name | LAMIVUDINE; ZIDOVUDINE |
| Strength Number | 150; 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] |
