NDC 55298-038 Titralac
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55298 - Inova Pharmaceuticals Pty, Ltd
- 55298-038 - Titralac
Product Characteristics
Product Packages
NDC Code 55298-038-10
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 55298-038?
What are the uses for Titralac?
Which are Titralac UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CALCIUM (UNII: SY7Q814VUP) (Active Moiety)
Which are Titralac 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:
- GLYCINE (UNII: TE7660XO1C)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SACCHARIN (UNII: FST467XS7D)
- SPEARMINT OIL (UNII: C3M81465G5)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Titralac?
- RxCUI: 313884 - calcium carbonate 420 MG (Ca 168 MG) Chewable Tablet
- RxCUI: 313884 - calcium carbonate 420 MG Chewable Tablet
- RxCUI: 313884 - calcium carbonate 420 MG (calcium 168 MG) Chewable Tablet
- RxCUI: 404179 - Titralac 420 MG (Ca 168 MG) Chewable Tablet
- RxCUI: 404179 - calcium carbonate 420 MG Chewable Tablet [Titralac]
* 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".