Package 50742-539-10

Brand: dehydrated alcohol

Generic: dehydrated alcohol
NDC Package

Package Facts

Identity

Package NDC 50742-539-10
Digits Only 5074253910
Product NDC 50742-539
Product ID 50742-539_149c50c5-59ad-4602-ad9e-58ad960eb91d
Description

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

Marketing

Marketing Status
Marketed Since 2025-07-09
Brand dehydrated alcohol
Generic dehydrated alcohol
Sample Package No

Linked Drug Pages (1)

Dehydrated Alcohol ndc-match (0.95)

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"}