Package 51991-999-17

Brand: dehydrated alcohol

Generic: alcohol
NDC Package

Package Facts

Identity

Package NDC 51991-999-17
Digits Only 5199199917
Product NDC 51991-999
Product ID 51991-999_7f58e5c6-78c9-471f-aef7-386b33a864d7
Description

10 VIAL, GLASS in 1 CARTON (51991-999-17) / 5 mL in 1 VIAL, GLASS (51991-999-75)

Marketing

Marketing Status
Marketed Since 2025-09-23
Brand dehydrated alcohol
Generic alcohol
Sample Package No

Linked Drug Pages (1)

Dehydrated Alcohol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRA-ARTERIAL"], "spl_id": "7f58e5c6-78c9-471f-aef7-386b33a864d7", "openfda": {"upc": ["0351991999171"], "unii": ["3K9958V90M"], "rxcui": ["2048982"], "spl_set_id": ["be10b253-d72a-4f57-aa27-94c70ae8aed3"], "manufacturer_name": ["Breckenridge Pharmaceutical Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, GLASS in 1 CARTON (51991-999-17)  / 5 mL in 1 VIAL, GLASS (51991-999-75)", "package_ndc": "51991-999-17", "marketing_start_date": "20250923"}], "brand_name": "Dehydrated Alcohol", "product_id": "51991-999_7f58e5c6-78c9-471f-aef7-386b33a864d7", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51991-999", "generic_name": "Alcohol", "labeler_name": "Breckenridge Pharmaceutical Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dehydrated Alcohol", "active_ingredients": [{"name": "ALCOHOL", "strength": "1 mL/mL"}], "application_number": "ANDA219444", "marketing_category": "ANDA", "marketing_start_date": "20250923", "listing_expiration_date": "20261231"}