dehydrated alcohol

Generic: alcohol

Labeler: xgen pharmaceuticals djb, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dehydrated alcohol
Generic Name alcohol
Labeler xgen pharmaceuticals djb, inc.
Dosage Form INJECTION, SOLUTION
Routes
PERCUTANEOUS
Active Ingredients

alcohol 1 mL/mL

Manufacturer
XGen Pharmaceuticals DJB, Inc.

Identifiers & Regulatory

Product NDC 39822-9300
Product ID 39822-9300_35a58769-c6cf-8c56-e063-6394a90a9857
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA219400
Listing Expiration 2026-12-31
Marketing Start 2025-06-24

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 398229300
Hyphenated Format 39822-9300

Supplemental Identifiers

RxCUI
2048982
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 alcohol (source: ndc)
Application Number ANDA219400 (source: ndc)
Routes
PERCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1 mL/mL
source: ndc
Packaging
  • 10 AMPULE in 1 CARTON (39822-9300-2) / 5 mL in 1 AMPULE (39822-9300-1)
source: ndc

Packages (1)

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

Ingredients (1)

alcohol (1 mL/mL)

Linked Drug Pages (1)

Dehydrated Alcohol ndc-match (0.9)

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"}