dehydrated alcohol

Generic: alcohol

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dehydrated alcohol
Generic Name alcohol
Labeler a-s medication solutions
Dosage Form INJECTION, SOLUTION
Routes
PERCUTANEOUS
Active Ingredients

alcohol 1 mL/mL

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7643
Product ID 50090-7643_3d1f5a98-a243-4cb4-b59d-6059ba0af173
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 500907643
Hyphenated Format 50090-7643

Supplemental Identifiers

RxCUI
2048982
UNII
3K9958V90M

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
  • 1 AMPULE in 1 CARTON (50090-7643-0) / 5 mL in 1 AMPULE
  • 2 AMPULE in 1 CARTON (50090-7643-1) / 5 mL in 1 AMPULE
source: ndc

Packages (2)

Ingredients (1)

alcohol (1 mL/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["PERCUTANEOUS"], "spl_id": "3d1f5a98-a243-4cb4-b59d-6059ba0af173", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["2048982"], "spl_set_id": ["ab8654b8-a4d5-4869-88c2-6a6cc5c77fff"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 AMPULE in 1 CARTON (50090-7643-0)  / 5 mL in 1 AMPULE", "package_ndc": "50090-7643-0", "marketing_start_date": "20250827"}, {"sample": false, "description": "2 AMPULE in 1 CARTON (50090-7643-1)  / 5 mL in 1 AMPULE", "package_ndc": "50090-7643-1", "marketing_start_date": "20250827"}], "brand_name": "Dehydrated Alcohol", "product_id": "50090-7643_3d1f5a98-a243-4cb4-b59d-6059ba0af173", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "50090-7643", "generic_name": "Alcohol", "labeler_name": "A-S Medication Solutions", "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"}