NDC 54868-6176 Urocit-k
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
RECTANGLE (C48347)
20 MM
M15
Code Structure Chart
Product Details
What is NDC 54868-6176?
What are the uses for Urocit-k?
Which are Urocit-k UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM CITRATE (UNII: EE90ONI6FF)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
Which are Urocit-k 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)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Urocit-k?
- 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
- RxCUI: 603281 - UROCIT-K 10 MEQ Extended Release Oral Tablet
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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".