United States · FDA National Drug Code directory
POSACONAZOLE
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
- 59651-596_c54279d9-ce17-4213-8db5-eee9bc63ea34
- Product NDC
- 59651-596
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- POSACONAZOLE
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240718
- Source listing expiry
- 20271231
Source-listed ingredients
- POSACONAZOLE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-596-60) · 59651-596-60
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 →