0990-7077 NDC - POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)

Drug Information

Product NDC: 0990-7077
Proprietary Name: Potassium Chloride
Non Proprietary Name: POTASSIUM CHLORIDE
Active Ingredient(s): 400 meq/1000mL POTASSIUM CHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Pharmacy Class(es): Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Potassium Compounds [CS]; Potassium Salt [EPC]

Labeler Information

Field Name	Field Value
Labeler Name:	ICU Medical Inc.
Product Type:	HUMAN PRESCRIPTION DRUG
FDA Application Number:	NDA020161
Marketing Category:	NDA
Start Marketing Date:	4/1/2019

Package Information

No.	Package Code	Package Description	Billing Unit
1	0990-7077-14	24 POUCH in 1 CASE (0990-7077-14) / 1 BAG in 1 POUCH / 50 mL in 1 BAG	ML
2	0990-7077-26	24 POUCH in 1 CASE (0990-7077-26) / 1 BAG in 1 POUCH / 100 mL in 1 BAG	ML

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	0990-7077	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.
PRODUCT TYPE NAME	HUMAN PRESCRIPTION DRUG	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
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.
NON PROPRIETARY NAME	POTASSIUM CHLORIDE	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.
DOSAGE FORM NAME	INJECTION, SOLUTION	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
ROUTE NAME	INTRAVENOUS	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
START MARKETING DATE	4/1/2019	The translation of the dosage form Code submitted by the firm.
MARKETING CATEGORY NAME	NDA	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.
APPLICATION NUMBER	NDA020161	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
LABELER NAME	ICU Medical Inc.	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
SUBSTANCE NAME	POTASSIUM CHLORIDE	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
ACTIVE NUMERATOR STRENGTH	400
ACTIVE INGRED UNIT	meq/1000mL
PHARM CLASSES	Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]

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This page was last updated on: 1/16/2026

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