NDC 50436-0621 Calcium Acetate
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What is NDC 50436-0621?
What are the uses for Calcium Acetate?
Which are Calcium Acetate UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM ACETATE (UNII: Y882YXF34X)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
Which are Calcium Acetate 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:
- CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Calcium Acetate?
- RxCUI: 197433 - calcium 169 MG Oral Tablet, as calcium acetate
- RxCUI: 197433 - calcium acetate 667 MG Oral Tablet
- RxCUI: 197433 - calcium acetate 667 MG (calcium 169 MG) 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".