dehydrated alcohol

Generic: alcohol

Labeler: breckenridge pharmaceutical inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dehydrated alcohol
Generic Name alcohol
Labeler breckenridge pharmaceutical inc
Dosage Form INJECTION, SOLUTION
Routes
INTRA-ARTERIAL
Active Ingredients

alcohol 1 mL/mL

Manufacturer
Breckenridge Pharmaceutical Inc

Identifiers & Regulatory

Product NDC 51991-999
Product ID 51991-999_7f58e5c6-78c9-471f-aef7-386b33a864d7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA219444
Listing Expiration 2026-12-31
Marketing Start 2025-09-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51991999
Hyphenated Format 51991-999

Supplemental Identifiers

RxCUI
2048982
UPC
0351991999171
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 ANDA219444 (source: ndc)
Routes
INTRA-ARTERIAL
source: ndc

Resolved Composition

Strengths
  • 1 mL/mL
source: ndc
Packaging
  • 10 VIAL, GLASS in 1 CARTON (51991-999-17) / 5 mL in 1 VIAL, GLASS (51991-999-75)
source: ndc

Packages (1)

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

Ingredients (1)

alcohol (1 mL/mL)

Linked Drug Pages (1)

Dehydrated Alcohol ndc-match (0.9)

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"}