Search Icon

59448-009 NDC - ETHYL ALCOHOL ()

Drug Information

Product NDC: 59448-009

Proprietary Name: ETHYL ALCOHOL

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: ASP Global, LLc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/18/2021

Package Information

No. Package Code Package Description Billing Unit
159448-009-0180 APPLICATOR in 1 PACKAGE (59448-009-01) / 5.2 mL in 1 APPLICATOR

NDC Record

Field Name Field Value Definition
PRODUCT NDC59448-009The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEETHYL ALCOHOLThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/18/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEASP Global, LLcName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023