United States · FDA National Drug Code directory
Dehydrated Alcohol
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
- 50742-539_149c50c5-59ad-4602-ad9e-58ad960eb91d
- Product NDC
- 50742-539
- Form
- INJECTION, SOLUTION
- Composition / generic term
- dehydrated alcohol
- Labeler
- Ingenus Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250709
- Source listing expiry
- 20261231
Source-listed ingredients
- DEHYDRATED ALCOHOL — 5 mL/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, GLASS in 1 CARTON (50742-539-10) / 5 mL in 1 VIAL, GLASS (50742-539-01) · 50742-539-10
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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