NDC 50742-539 – Dehydrated Alcohol

Dehydrated Alcohol 5 mL/5mL · Injection, Solution · Percutaneous

Human Prescription Drug

Product NDC50742-539

Product details

Brand name
Dehydrated Alcohol
Generic name
Dehydrated alcohol
Labeler
Ingenus Pharmaceuticals, LLC
Dosage form
Injection, Solution
Route
Percutaneous
Marketing category
ANDA · ANDA219569
Marketed since
July 9, 2025
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Dehydrated Alcohol →

Package NDC codes (1)

Package NDCDescriptionSince
50742-539-1010 VIAL, GLASS in 1 CARTON (50742-539-10) / 5 mL in 1 VIAL, GLASS (50742-539-01)Jul 9, 2025

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