| NDC Code: |
24236-292 |
| Proprietary Name: |
Atripla |
| Suffix: |
|
| Non-Proprietary Name: |
efavirenz, emtricitabine, and tenofovir disoproxil fumarate |
| Dosage Form: |
TABLET, FILM COATED |
| Method: |
ORAL |
| Original Marketing Date: |
29-03-2013 |
| Category Name: |
NDA |
| Application Number: |
NDA021937 |
| Labeler: |
REMEDYREPACK INC. |
| Substance Name: |
EFAVIRENZ |
| Active Numerator Strength: |
600 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [Chemical/Ingredient],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA] |
| DEA Schedule: |
|
