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
59651-086_2b5403e0-28fe-44ef-9b80-f754181ba220
Product NDC
59651-086
Form
TABLET, FILM COATED
Composition / generic term
Darunavir
Labeler
Aurobindo Pharma Limited
Marketing category
ANDA
Marketing start / end (source format)
20231128
Source listing expiry
20261231

Source-listed ingredients

  • DARUNAVIR PROPYLENE GLYCOLATE — 800 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED in 1 BOTTLE (59651-086-30) · 59651-086-30

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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