58118-1526 NDC - POTASSIUM CHLORIDE ()

Drug Information

Product NDC: 58118-1526

Proprietary Name: Potassium Chloride

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Clinical Solutions Wholesale
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	4/17/1986

No.	Package Code	Package Description	Billing Unit
1	58118-1526-8	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (58118-1526-8)

Field Name	Field Value	Definition
PRODUCT NDC	58118-1526	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	4/17/1986	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Clinical Solutions Wholesale	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024