# Emtricitabine and Tenofovir Disoproxil Fumarate

NDC: 0093-7704
Generic name: Emtricitabine and Tenofovir Disoproxil Fumarate
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210120

FDA application: ANDA090894

## Active ingredients

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

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-7704"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-7704
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e1e4d828-7870-4ea9-a66a-e658487bd859