76063-738 NDC - HANDI-SANI ()

Drug Information

Product NDC: 76063-738

Proprietary Name: Handi-Sani

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Chromate Industrial Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	2/1/2011

No.	Package Code	Package Description
1	76063-738-14	3785 mL in 1 BOTTLE, PLASTIC (76063-738-14)
2	76063-738-15	946 mL in 1 BOTTLE, PLASTIC (76063-738-15)
3	76063-738-16	236 mL in 1 BOTTLE, PLASTIC (76063-738-16)
4	76063-738-17	532 mL in 1 BOTTLE, PLASTIC (76063-738-17)
5	76063-738-18	50 mL in 1 BOTTLE, PLASTIC (76063-738-18)
6	76063-738-24	118 mL in 1 BOTTLE, PLASTIC (76063-738-24)
7	76063-738-55	208200 mL in 1 DRUM (76063-738-55)

Field Name	Field Value	Definition
PRODUCT NDC	76063-738	The 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 NAME	Handi-Sani	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	2/1/2011	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Chromate Industrial Corporation	Name of Company corresponding to the labeler code segment of the Product NDC.

Export to text format icon Download this NDC record in Text format: Export

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

Export to text format icon Download this NDC record in XML format: Export

This page was last updated on: 5/3/2024