United States · FDA National Drug Code directory
Darunavir 600 and 800 mg
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
- 63629-5686_290dd3c3-c6b7-415f-99b3-680080281b30
- Product NDC
- 63629-5686
- Form
- TABLET
- Composition / generic term
- darunavir
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231129
- Source listing expiry
- 20261231
Source-listed ingredients
- DARUNAVIR DIHYDRATE — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET in 1 BOTTLE (63629-5686-1) · 63629-5686-1
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →