dehydrated alcohol
Generic: alcohol
Labeler: ajenat pharmaceuticals llcDrug Facts
Product Profile
Brand Name
dehydrated alcohol
Generic Name
alcohol
Labeler
ajenat pharmaceuticals llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
alcohol 1 mL/mL
Manufacturer
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
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 1 mL/mL
Packaging
- 10 VIAL in 1 CARTON (82983-426-10) / 5 mL in 1 VIAL (82983-426-01)
Packages (1)
Ingredients (1)
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"}