NDC Code |
35356-064-30 |
Proprietary Name |
Atripla |
Package Description |
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (35356-064-30) |
Product NDC |
35356-064 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
efavirenz, emtricitabine, and tenofovir disoproxil fumarate |
Dosage Form Name |
TABLET, FILM COATED |
Route Name |
ORAL |
Start Marketing Date |
20060720 |
Marketing Category Name |
NDA |
Labeler Name |
Lake Erie Medical DBA Quality Care Products LLC |
Substance Name |
EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE |
Strength Number |
600; 200; 300 |
Strength Unit |
mg/1; mg/1; mg/1 |
Pharmaceutical Classes |
Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [Chemical/Ingredient],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA],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] |