NDC 65162-542 Potassium Chloride
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Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 65162-542?
What are the uses for Potassium Chloride?
Which are Potassium Chloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
Which are Potassium Chloride 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:
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- GELATIN (UNII: 2G86QN327L)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Potassium Chloride?
- RxCUI: 312504 - potassium chloride 10 MEQ Extended Release Oral Capsule
- RxCUI: 312504 - K+ Chloride 10 MEQ Extended Release Oral Capsule
- RxCUI: 312504 - Pot Chloride 10 MEQ Extended Release Oral Capsule
- RxCUI: 312504 - potassium chloride 750 MG Extended Release Oral Capsule
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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".