United States · FDA National Drug Code directory
Darunavir
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
- 72578-147_de3be678-a82f-4052-b7ce-728d887d548e
- Product NDC
- 72578-147
- Form
- TABLET, FILM COATED
- Composition / generic term
- Darunavir
- Labeler
- Viona Pharmaceuticals Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240501
- Source listing expiry
- 20261231
Source-listed ingredients
- DARUNAVIR — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET, FILM COATED in 1 BOTTLE (72578-147-05) · 72578-147-05
- 60 TABLET, FILM COATED in 1 BOTTLE (72578-147-14) · 72578-147-14
- 180 TABLET, FILM COATED in 1 BOTTLE (72578-147-28) · 72578-147-28
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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