dehydrated alcohol

Generic: alcohol

Labeler: ajenat pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

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

alcohol 1 mL/mL

Manufacturer
Ajenat Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 82983-426
Product ID 82983-426_be0bec74-c6a7-49e7-931f-69d289cb366f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA207987
Listing Expiration 2026-12-31
Marketing Start 2025-08-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82983426
Hyphenated Format 82983-426

Supplemental Identifiers

RxCUI
2048982
UPC
0382983426108 0382983426016
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 NDA207987 (source: ndc)
Routes
PERCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1 mL/mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (82983-426-10) / 5 mL in 1 VIAL (82983-426-01)
source: ndc

Packages (1)

Ingredients (1)

alcohol (1 mL/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["PERCUTANEOUS"], "spl_id": "be0bec74-c6a7-49e7-931f-69d289cb366f", "openfda": {"upc": ["0382983426108", "0382983426016"], "unii": ["3K9958V90M"], "rxcui": ["2048982"], "spl_set_id": ["636d6421-cadf-42b3-a431-ba40c06e36d2"], "manufacturer_name": ["Ajenat Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (82983-426-10)  / 5 mL in 1 VIAL (82983-426-01)", "package_ndc": "82983-426-10", "marketing_start_date": "20250815"}], "brand_name": "Dehydrated Alcohol", "product_id": "82983-426_be0bec74-c6a7-49e7-931f-69d289cb366f", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "82983-426", "generic_name": "Alcohol", "labeler_name": "Ajenat Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dehydrated Alcohol", "active_ingredients": [{"name": "ALCOHOL", "strength": "1 mL/mL"}], "application_number": "NDA207987", "marketing_category": "NDA", "marketing_start_date": "20250815", "listing_expiration_date": "20261231"}