dehydrated alcohol

Generic: alcohol

Labeler: accord healthcare, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dehydrated alcohol
Generic Name alcohol
Labeler accord healthcare, inc.
Dosage Form INJECTION, SOLUTION
Routes
PERCUTANEOUS
Active Ingredients

alcohol 1 mL/mL

Manufacturer
Accord Healthcare, Inc.

Identifiers & Regulatory

Product NDC 16729-710
Product ID 16729-710_386b65ee-b908-0daf-e063-6394a90a9bbb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217845
Listing Expiration 2026-12-31
Marketing Start 2025-06-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16729710
Hyphenated Format 16729-710

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 ANDA217845 (source: ndc)
Routes
PERCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1 mL/mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (16729-710-45) / 5 mL in 1 VIAL (16729-710-31)
source: ndc

Packages (1)

Ingredients (1)

alcohol (1 mL/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["PERCUTANEOUS"], "spl_id": "386b65ee-b908-0daf-e063-6394a90a9bbb", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["2048982"], "spl_set_id": ["07fa92f7-d752-42e3-a572-b552461c4389"], "manufacturer_name": ["Accord Healthcare, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (16729-710-45)  / 5 mL in 1 VIAL (16729-710-31)", "package_ndc": "16729-710-45", "marketing_start_date": "20250625"}], "brand_name": "DEHYDRATED ALCOHOL", "product_id": "16729-710_386b65ee-b908-0daf-e063-6394a90a9bbb", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "16729-710", "generic_name": "ALCOHOL", "labeler_name": "Accord Healthcare, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEHYDRATED ALCOHOL", "active_ingredients": [{"name": "ALCOHOL", "strength": "1 mL/mL"}], "application_number": "ANDA217845", "marketing_category": "ANDA", "marketing_start_date": "20250625", "listing_expiration_date": "20261231"}