NDC 71335-1706 Potassium Citrate Extended Release
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71335 - Bryant Ranch Prepack
- 71335-1706 - Potassium Citrate
Product Characteristics
Product Packages
NDC Code 71335-1706-1
Package Description: 30 TABLET in 1 BOTTLE
Product Details
What is NDC 71335-1706?
What are the uses for Potassium Citrate Extended Release?
Which are Potassium Citrate Extended Release UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM CITRATE (UNII: EE90ONI6FF)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (Active Moiety)
Which are Potassium Citrate Extended Release 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:
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Potassium Citrate Extended Release?
- RxCUI: 199381 - potassium citrate 10 MEQ Extended Release Oral Tablet
- RxCUI: 199381 - K+ citrate 10 MEQ Extended Release Oral Tablet
- RxCUI: 199381 - Pot citrate 10 MEQ Extended Release Oral Tablet
- RxCUI: 199381 - potassium citrate 1080 MG 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".