United States · FDA National Drug Code directory
voriconazole
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
- 70436-029_5134712f-f9ea-09cf-e063-6294a90addf1
- Product NDC
- 70436-029
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- voriconazole
- Labeler
- Slate Run Pharmaceuticals
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190128
- Source listing expiry
- 20271231
Source-listed ingredients
- VORICONAZOLE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 BOX (70436-029-80) · 70436-029-80
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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