NDC 53808-1103 Calcium Acetate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - Doh Central Pharmacy
- 53808-1103 - Calcium Acetate
Product Characteristics
Product Packages
NDC Code 53808-1103-1
Package Description: 30 CAPSULE in 1 BLISTER PACK
Product Details
What is NDC 53808-1103?
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:
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Calcium Acetate?
- RxCUI: 359296 - calcium acetate 667 MG (Ca 169 MG) Oral Capsule
- RxCUI: 359296 - calcium acetate 667 MG Oral Capsule
- RxCUI: 359296 - calcium acetate 667 MG (calcium 169 MG) Oral Capsule
* Please review the disclaimer below.
Patient Education
Calcium Acetate
Calcium acetate is used to control high blood levels of phosphorus in people with kidney disease who are on dialysis (medical treatment to clean the blood when the kidneys are not working properly). Calcium acetate is in a class of medications called phosphate binders. It binds phosphorus that you get from foods in your diet and prevents it from being absorbed into your blood stream.
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* Please review the disclaimer below.
[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".