United States · FDA National Drug Code directory
Tenofovir Disoproxil Fumarate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 71921-105_79278443-b9ee-4db6-ac15-a3d12b359eb0
- Product NDC
- 71921-105
- Form
- TABLET, COATED
- Composition / generic term
- Tenofovir Disoproxil Fumarate
- Labeler
- Florida Pharmaceutical Products, LLC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251126
- Source listing expiry
- 20261231
Source-listed ingredients
- TENOFOVIR DISOPROXIL FUMARATE — 300 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, COATED in 1 BOTTLE, PLASTIC (71921-105-33) · 71921-105-33
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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