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
71335-3155_1d924bad-47a1-48dd-bf2e-5a44ebc48d60
Product NDC
71335-3155
Form
TABLET, COATED
Composition / generic term
Tenofovir Disoproxil Fumarate
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20251126
Source listing expiry
20271231

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 (71335-3155-1) · 71335-3155-1
  • 15 TABLET, COATED in 1 BOTTLE, PLASTIC (71335-3155-2) · 71335-3155-2

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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Tenofovir Disoproxil Fumarate — United States | Molindra Medicines