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Truvada
Truvada - 52959-969-03 - (emtricitabine and tenofovir disoproxil fumarate)
Drug Information of Truvada
| Product NDC: | 52959-969 |
| 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: | 52959-969 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021752 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20040802 |
Package Information of Truvada
| Package NDC: | 52959-969-03 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52959-969-03) |
NDC Information of Truvada
| NDC Code | 52959-969-03 |
| Proprietary Name | Truvada |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52959-969-03) |
| Product NDC | 52959-969 |
| 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 | 20040802 |
| Marketing Category Name | NDA |
| Labeler Name | H.J. Harkins Company, Inc. |
| 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] |
