dehydrated alcohol

Generic: dehydrated alcohol

Labeler: ingenus pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dehydrated alcohol
Generic Name dehydrated alcohol
Labeler ingenus pharmaceuticals, llc
Dosage Form INJECTION, SOLUTION
Routes
PERCUTANEOUS
Active Ingredients

dehydrated alcohol 5 mL/5mL

Manufacturer
Ingenus Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 50742-539
Product ID 50742-539_149c50c5-59ad-4602-ad9e-58ad960eb91d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA219569
Listing Expiration 2026-12-31
Marketing Start 2025-07-09

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50742539
Hyphenated Format 50742-539

Supplemental Identifiers

RxCUI
2048982
UPC
0350742539017
UNII
3K9958V90M

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name dehydrated alcohol (source: ndc)
Generic Name dehydrated alcohol (source: ndc)
Application Number ANDA219569 (source: ndc)
Routes
PERCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 5 mL/5mL
source: ndc
Packaging
  • 10 VIAL, GLASS in 1 CARTON (50742-539-10) / 5 mL in 1 VIAL, GLASS (50742-539-01)
source: ndc

Packages (1)

50742-539-10 10 VIAL, GLASS in 1 CARTON (50742-539-10) / 5 mL in 1 VIAL, GLASS (50742-539-01)

Ingredients (1)

dehydrated alcohol (5 mL/5mL)

Linked Drug Pages (1)

Dehydrated Alcohol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["PERCUTANEOUS"], "spl_id": "149c50c5-59ad-4602-ad9e-58ad960eb91d", "openfda": {"upc": ["0350742539017"], "unii": ["3K9958V90M"], "rxcui": ["2048982"], "spl_set_id": ["1d5ec6f9-d58f-4651-a4a1-93fec13fd438"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, GLASS in 1 CARTON (50742-539-10)  / 5 mL in 1 VIAL, GLASS (50742-539-01)", "package_ndc": "50742-539-10", "marketing_start_date": "20250709"}], "brand_name": "Dehydrated Alcohol", "product_id": "50742-539_149c50c5-59ad-4602-ad9e-58ad960eb91d", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "50742-539", "generic_name": "dehydrated alcohol", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dehydrated Alcohol", "active_ingredients": [{"name": "DEHYDRATED ALCOHOL", "strength": "5 mL/5mL"}], "application_number": "ANDA219569", "marketing_category": "ANDA", "marketing_start_date": "20250709", "listing_expiration_date": "20261231"}