Package 39822-9300-2

Brand: dehydrated alcohol

Generic: alcohol
NDC Package

Package Facts

Identity

Package NDC 39822-9300-2
Digits Only 3982293002
Product NDC 39822-9300
Product ID 39822-9300_35a58769-c6cf-8c56-e063-6394a90a9857
Description

10 AMPULE in 1 CARTON (39822-9300-2) / 5 mL in 1 AMPULE (39822-9300-1)

Marketing

Marketing Status
Marketed Since 2025-06-24
Brand dehydrated alcohol
Generic 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": "35a58769-c6cf-8c56-e063-6394a90a9857", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["2048982"], "spl_set_id": ["35a568f3-83cd-452e-e063-6394a90a8c1d"], "manufacturer_name": ["XGen Pharmaceuticals DJB, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 CARTON (39822-9300-2)  / 5 mL in 1 AMPULE (39822-9300-1)", "package_ndc": "39822-9300-2", "marketing_start_date": "20250624"}], "brand_name": "Dehydrated Alcohol", "product_id": "39822-9300_35a58769-c6cf-8c56-e063-6394a90a9857", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "39822-9300", "generic_name": "Alcohol", "labeler_name": "XGen Pharmaceuticals DJB, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dehydrated Alcohol", "active_ingredients": [{"name": "ALCOHOL", "strength": "1 mL/mL"}], "application_number": "ANDA219400", "marketing_category": "ANDA", "marketing_start_date": "20250624", "listing_expiration_date": "20261231"}