NDC 48083-305 Certi-antacid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 48083-305-27
Package Description: 25 POUCH in 1 BOX / 2 TABLET in 1 POUCH
NDC Code 48083-305-30
Package Description: 50 POUCH in 1 BOX / 2 TABLET in 1 POUCH
NDC Code 48083-305-31
Package Description: 50 POUCH in 1 BOX / 2 TABLET in 1 POUCH
NDC Code 48083-305-33
Package Description: 125 POUCH in 1 BOX / 2 TABLET in 1 POUCH
NDC Code 48083-305-36
Package Description: 250 POUCH in 1 BOX / 2 TABLET in 1 POUCH
NDC Code 48083-305-39
Package Description: 500 POUCH in 1 BOX / 2 TABLET in 1 POUCH
NDC Code 48083-305-41
Package Description: 1000 POUCH in 1 BOX / 2 TABLET in 1 POUCH
Product Details
What is NDC 48083-305?
What are the uses for Certi-antacid?
Which are Certi-antacid UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
Which are Certi-antacid 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:
- ASPARTAME (UNII: Z0H242BBR1)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MINT (UNII: FV98Z8GITP)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Certi-antacid?
- RxCUI: 198529 - calcium carbonate 420 MG (Ca 168 MG) Oral Tablet
- RxCUI: 198529 - calcium carbonate 420 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".