NDC 49789-060 His Ulc Mint Blue
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49789 - Samsung Pharm Ind. Co., Ltd.
- 49789-060 - His Ulc Mint Blue
Product Characteristics
Product Packages
NDC Code 49789-060-01
Package Description: 492 mg in 1 BLISTER PACK
Product Details
What is NDC 49789-060?
What are the uses for His Ulc Mint Blue?
Which are His Ulc Mint Blue UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
Which are His Ulc Mint Blue 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:
- MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)
- ASPARTAME (UNII: Z0H242BBR1)
What is the NDC to RxNorm Crosswalk for His Ulc Mint Blue?
- RxCUI: 204637 - calcium carbonate 350 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".