NDC 0603-4170 K-effervescent

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
0603-4170
Proprietary Name:
K-effervescent
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Qualitest Pharmaceuticals
Labeler Code:
0603
Start Marketing Date: [9]
01-06-2006
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
Shape:
ROUND (C48348)
Size(s):
25 MM
Imprint(s):
T
Score:
2
Flavor(s):
ORANGE (C73406 - NATURAL ORANGE FLAVOR NV-3103)

Product Packages

NDC Code 0603-4170-16

Package Description: 30 TABLET, EFFERVESCENT in 1 BOX

Price per Unit: $0.19693 per EA

Product Details

What is NDC 0603-4170?

The NDC code 0603-4170 is assigned by the FDA to the product K-effervescent which is product labeled by Qualitest Pharmaceuticals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0603-4170-16 30 tablet, effervescent in 1 box . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for K-effervescent?

INDICATIONS AN USAGE:1. For therapeutic use in patients with hypokalemia with or without metabolic alkalosis; in digitalis intoxication and in patients with hypokalemic familial    periodic paralysis.2. For prevention of potassium depletion when the dietary intake of potassium is inadequate in the following conditions; patients receiving digitalis and    diuretics for congestive heart failure; hepatic cirrhosis with ascites; states of aldosterone excess with normal renal function; potassium-losing    nephropathy, and certain diarrheal states.3. The use of potassium salts in patients receiving diuretics for uncomplicated essential hypertension is often unnecessary when such patients have a    normal dietary pattern.  Serum potassium should be checked periodically, however, and, if hypokalemia occurs, dietary supplementation with    potassium-containing foods may be adequate to control milder cases.  In more severe cases supplementation with potassium salts may be    indicated.

Which are K-effervescent UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are K-effervescent Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for K-effervescent?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".