72322-1032 NDC - POTASSIUM CHLORIDE ()

Drug Information

Product NDC: 72322-1032

Proprietary Name: Potassium Chloride

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	72322-1032-1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72322-1032-1)
2	72322-1032-2	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72322-1032-2)
3	72322-1032-3	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72322-1032-3)

Field Name	Field Value	Definition
PRODUCT NDC	72322-1032	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	Potassium Chloride	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	12/20/2021	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	AMTA LABS LIMITED	Name 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