70518-2313 NDC - POTASSIUM CHLORIDE ()

Drug Information

Product NDC: 70518-2313

Proprietary Name: Potassium Chloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: REMEDYREPACK INC.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/13/2019

Package Information

No. Package Code Package Description Billing Unit
170518-2313-030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2313-0)
270518-2313-190 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2313-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC70518-2313The 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 NAMEPotassium ChlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/13/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEREMEDYREPACK INC.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