# Truvada

NDC: 68071-2112
Generic name: emtricitabine and tenofovir disoproxil fumarate
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20040802

FDA application: NDA021752

## Active ingredients

- EMTRICITABINE: 200 mg/1
- TENOFOVIR DISOPROXIL FUMARATE: 300 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-2112"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-2112
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=46e06df0-654d-43cc-e054-00144ff8d46c