Package 50090-7643-0

Brand: dehydrated alcohol

Generic: alcohol
NDC Package

Package Facts

Identity

Package NDC 50090-7643-0
Digits Only 5009076430
Product NDC 50090-7643
Description

1 AMPULE in 1 CARTON (50090-7643-0) / 5 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2025-08-27
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": "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"}