Drugplain

Truvada 200 mg/1

emtricitabine and tenofovir disoproxil fumarate · TABLET, FILM COATED · Gilead Sciences, Inc

No Recall History
Plain English

Truvada is a tablet, film coated containing emtricitabine and tenofovir disoproxil fumarate at 200 mg/1, taken oral. Manufactured by Gilead Sciences, Inc.

Key Facts

Brand Name
Truvada
Generic Name
emtricitabine and tenofovir disoproxil fumarate
NDC Code (Product)
61958-0701
Manufacturer
Gilead Sciences, Inc
Strength
200 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
NDA021752
Drug Class
Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
Marketing Start
08/02/2004

Recall History

No Recall History

Frequently Asked Questions

What is Truvada used for?

Truvada contains emtricitabine and tenofovir disoproxil fumarate. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is Truvada a controlled substance?

Truvada is not classified as a controlled substance by the DEA.

What is the generic name for Truvada?

The generic name for Truvada is emtricitabine and tenofovir disoproxil fumarate. There are 12 other brand versions of emtricitabine and tenofovir disoproxil fumarate.

What is the NDC code for Truvada 200 mg/1?

The NDC (National Drug Code) for Truvada 200 mg/1 is 61958-0701, listed by Gilead Sciences, Inc.