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Emtriva
Emtriva - 61958-0602-1 - (EMTRICITABINE)
Drug Information of Emtriva
| Product NDC: | 61958-0602 |
| Proprietary Name: | Emtriva |
| Non Proprietary Name: | EMTRICITABINE |
| Active Ingredient(s): | 10 mg/mL & nbsp; EMTRICITABINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Emtriva
| Product NDC: | 61958-0602 |
| Labeler Name: | Gilead Sciences, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021896 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050928 |
Package Information of Emtriva
| Package NDC: | 61958-0602-1 |
| Package Description: | 1 BOTTLE, DISPENSING in 1 CARTON (61958-0602-1) > 170 mL in 1 BOTTLE, DISPENSING |
NDC Information of Emtriva
| NDC Code | 61958-0602-1 |
| Proprietary Name | Emtriva |
| Package Description | 1 BOTTLE, DISPENSING in 1 CARTON (61958-0602-1) > 170 mL in 1 BOTTLE, DISPENSING |
| Product NDC | 61958-0602 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | EMTRICITABINE |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20050928 |
| Marketing Category Name | NDA |
| Labeler Name | Gilead Sciences, Inc. |
| Substance Name | EMTRICITABINE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
