62712-575 NDC - HANDI-SAN ()

Drug Information

Product NDC: 62712-575

Proprietary Name: Handi-San

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Atco International
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/2006

Package Information

No. Package Code Package Description Billing Unit
162712-575-101000 mL in 1 CARTRIDGE (62712-575-10)
262712-575-121000 mL in 1 BAG (62712-575-12)
362712-575-13800 mL in 1 BAG (62712-575-13)
462712-575-143785 mL in 1 BOTTLE, PLASTIC (62712-575-14)
562712-575-15946 mL in 1 BOTTLE, PLASTIC (62712-575-15)
662712-575-16236 mL in 1 BOTTLE, PLASTIC (62712-575-16)
762712-575-17532 mL in 1 BOTTLE, PLASTIC (62712-575-17)
862712-575-1850 mL in 1 BOTTLE, PLASTIC (62712-575-18)
962712-575-24115 mL in 1 BOTTLE, PLASTIC (62712-575-24)
1062712-575-27800 mL in 1 CARTRIDGE (62712-575-27)
1162712-575-55208200 mL in 1 DRUM (62712-575-55)

NDC Record

Field Name Field Value Definition
PRODUCT NDC62712-575The 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 NAMEHandi-SanThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/1/2006This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAtco InternationalName of Company corresponding to the labeler code segment of the Product NDC.

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