# TENOFOVIR DISOPROXIL FUMARATE

NDC: 64380-714
Generic name: tenofovir disoproxil fumarate
Labeler / Manufacturer: Strides Pharma Science Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180126

FDA application: ANDA090742

## Active ingredients

- 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:"64380-714"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64380-714
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bcd3120b-60f6-41d8-a512-ed4a62c836b4