# Emtricitabine and tenofovir disoproxil fumarate

NDC: 16714-534
Generic name: Emtricitabine and tenofovir disoproxil fumarate
Labeler / Manufacturer: NorthStar RxLLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220309

FDA application: ANDA203442

## 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:"16714-534"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-534
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fbbc7b73-eddf-40b5-8ebb-7b3d9c42dba6