NDC 0536-1049 Calcium Antacidextra Strength Extra Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
GREEN (C48329)
RED (C48326)
ORANGE (C48331)
Code Structure Chart
Product Details
What is NDC 0536-1049?
What are the uses for Calcium Antacidextra Strength Extra Strength?
Which are Calcium Antacidextra Strength Extra Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
Which are Calcium Antacidextra Strength Extra Strength 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:
- ADIPIC ACID (UNII: 76A0JE0FKJ)
- DEXTROSE (UNII: IY9XDZ35W2)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STARCH, CORN (UNII: O8232NY3SJ)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Calcium Antacidextra Strength Extra Strength?
- RxCUI: 308915 - calcium carbonate 750 MG (Ca 300 MG) Chewable Tablet
- RxCUI: 308915 - calcium carbonate 750 MG Chewable Tablet
- RxCUI: 308915 - calcium carbonate 750 MG (calcium 300 MG) Chewable 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".