Product NDC: | 61958-0601 |
Proprietary Name: | Emtriva |
Non Proprietary Name: | EMTRICITABINE |
Active Ingredient(s): | 200 mg/1 & nbsp; EMTRICITABINE |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61958-0601 |
Labeler Name: | Gilead Sciences, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021500 |
Marketing Category: | NDA |
Start Marketing Date: | 20030702 |
Package NDC: | 61958-0601-1 |
Package Description: | 30 CAPSULE in 1 BOTTLE, PLASTIC (61958-0601-1) |
NDC Code | 61958-0601-1 |
Proprietary Name | Emtriva |
Package Description | 30 CAPSULE in 1 BOTTLE, PLASTIC (61958-0601-1) |
Product NDC | 61958-0601 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | EMTRICITABINE |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20030702 |
Marketing Category Name | NDA |
Labeler Name | Gilead Sciences, Inc. |
Substance Name | EMTRICITABINE |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |