United States · FDA National Drug Code directory
Docosanol
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
- 73581-004_57118a58-dfdd-6764-e063-6394a90aebb6
- Product NDC
- 73581-004
- Form
- CREAM
- Composition / generic term
- Docosanol
- Labeler
- YYBA Corp
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250326
- Source listing expiry
- 20271231
Source-listed ingredients
- DOCOSANOL — 100 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TUBE in 1 PACKAGE (73581-004-02) / 2 g in 1 TUBE · 73581-004-02
- 1 TUBE in 1 PACKAGE (73581-004-03) / 2 g in 1 TUBE · 73581-004-03
- 1 TUBE in 1 CARTON (73581-004-10) / 1 g in 1 TUBE · 73581-004-10
- 2 TUBE in 1 CARTON (73581-004-20) / 2 g in 1 TUBE · 73581-004-20
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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