NDC 51655-587 Potassium Chloride ER
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51655 - Northwind Pharmaceuticals
- 51655-587 - Potassium Chloride
Product Characteristics
Product Packages
NDC Code 51655-587-52
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, DISPENSING
Product Details
What is NDC 51655-587?
What are the uses for Potassium Chloride ER?
Which are Potassium Chloride ER UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Potassium Chloride ER?
- RxCUI: 628953 - potassium chloride 10 MEQ (750 MG) Extended Release Oral Tablet
- RxCUI: 628953 - potassium chloride 10 MEQ Extended Release Oral Tablet
- RxCUI: 628953 - K+ Chloride 10 MEQ Extended Release Oral Tablet
- RxCUI: 628953 - Pot Chloride 10 MEQ Extended Release Oral Tablet
- RxCUI: 628953 - potassium chloride 750 MG (potassium 10 mEq) Extended Release Oral Tablet
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Patient Education
Potassium
Potassium is essential for the proper functioning of the heart, kidneys, muscles, nerves, and digestive system. Usually the food you eat supplies all of the potassium you need. However, certain diseases (e.g., kidney disease and gastrointestinal disease with vomiting and diarrhea) and drugs, especially diuretics ('water pills'), remove potassium from the body. Potassium supplements are taken to replace potassium losses and prevent potassium deficiency. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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[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".