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
- 70748-258_ef76e94c-f183-4eef-8fee-a52635cdcd34
- Product NDC
- 70748-258
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- POSACONAZOLE
- Labeler
- Lupin Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210217
- 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 (70748-258-07) · 70748-258-07
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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