dehydrated alcohol

Generic: alcohol

Labeler: solupharm pharmazeutische erzeugnisse gmbh
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dehydrated alcohol
Generic Name alcohol
Labeler solupharm pharmazeutische erzeugnisse gmbh
Dosage Form INJECTION
Routes
PERCUTANEOUS
Active Ingredients

alcohol 1 mL/mL

Manufacturer
Solupharm Pharmazeutische Erzeugnisse GmbH

Identifiers & Regulatory

Product NDC 55579-306
Product ID 55579-306_462e1f5b-024d-3dcb-e063-6294a90a9520
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA219569
Listing Expiration 2026-12-31
Marketing Start 2025-01-08

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55579306
Hyphenated Format 55579-306

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 ANDA219569 (source: ndc)
Routes
PERCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1 mL/mL
source: ndc
Packaging
  • 5 mL in 1 BOX (55579-306-05)
  • 5 mL in 1 VIAL, SINGLE-USE (55579-306-41)
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": "462e1f5b-024d-3dcb-e063-6294a90a9520", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["2048982"], "spl_set_id": ["372d3eb5-78ee-414c-a146-4a19e2266184"], "manufacturer_name": ["Solupharm Pharmazeutische Erzeugnisse GmbH"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 BOX (55579-306-05)", "package_ndc": "55579-306-05", "marketing_start_date": "20250108"}, {"sample": false, "description": "5 mL in 1 VIAL, SINGLE-USE (55579-306-41)", "package_ndc": "55579-306-41", "marketing_start_date": "20250108"}], "brand_name": "Dehydrated Alcohol", "product_id": "55579-306_462e1f5b-024d-3dcb-e063-6294a90a9520", "dosage_form": "INJECTION", "product_ndc": "55579-306", "generic_name": "ALCOHOL", "labeler_name": "Solupharm Pharmazeutische Erzeugnisse GmbH", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dehydrated Alcohol", "active_ingredients": [{"name": "ALCOHOL", "strength": "1 mL/mL"}], "application_number": "ANDA219569", "marketing_category": "ANDA", "marketing_start_date": "20250108", "listing_expiration_date": "20261231"}