Package 55579-306-41
Brand: dehydrated alcohol
Generic: alcoholPackage Facts
Identity
Package NDC
55579-306-41
Digits Only
5557930641
Product NDC
55579-306
Description
5 mL in 1 VIAL, SINGLE-USE (55579-306-41)
Marketing
Marketing Status
Brand
dehydrated alcohol
Generic
alcohol
Sample Package
No
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"}