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Truvada
Truvada - 53808-0805-1 - (emtricitabine and tenofovir disoproxil fumarate)
Drug Information of Truvada
| Product NDC: | 53808-0805 |
| Proprietary Name: | Truvada |
| Non Proprietary Name: | emtricitabine and tenofovir disoproxil fumarate |
| Active Ingredient(s): | 200; 300 mg/1; mg/1 & nbsp; emtricitabine and tenofovir disoproxil fumarate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Truvada
| Product NDC: | 53808-0805 |
| Labeler Name: | State of Florida DOH Central Pharmacy |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021752 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090701 |
Package Information of Truvada
| Package NDC: | 53808-0805-1 |
| Package Description: | 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0805-1) |
NDC Information of Truvada
| NDC Code | 53808-0805-1 |
| Proprietary Name | Truvada |
| Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0805-1) |
| Product NDC | 53808-0805 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | emtricitabine and tenofovir disoproxil fumarate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090701 |
| Marketing Category Name | NDA |
| Labeler Name | State of Florida DOH Central Pharmacy |
| Substance Name | EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE |
| Strength Number | 200; 300 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
