51477-002 NDC - POTASSIUM CHLORIDE ()

Drug Information

Product NDC: 51477-002

Proprietary Name: potassium chloride

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Nesher Pharmaceuticals (USA) LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	10/25/2010

No.	Package Code	Package Description	Billing Unit
1	51477-002-03	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51477-002-03)
2	51477-002-04	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51477-002-04)

Field Name	Field Value	Definition
PRODUCT NDC	51477-002	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	10/25/2010	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Nesher Pharmaceuticals (USA) LLC	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