NDC 53808-0957 Pantoprazole Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - State Of Florida Doh Central Pharmacy
- 53808-0957 - Pantoprazole Sodium
Product Characteristics
Product Packages
NDC Code 53808-0957-1
Package Description: 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product Details
What is NDC 53808-0957?
What are the uses for Pantoprazole Sodium?
Which are Pantoprazole Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- PANTOPRAZOLE SODIUM (UNII: 6871619Q5X)
- PANTOPRAZOLE (UNII: D8TST4O562) (Active Moiety)
Which are Pantoprazole Sodium 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:
- AMMONIA (UNII: 5138Q19F1X)
- DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER (UNII: 905HNO1SIH)
- CALCIUM STEARATE (UNII: 776XM7047L)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- MANNITOL (UNII: 3OWL53L36A)
- METHACRYLIC ACID (UNII: 1CS02G8656)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Pantoprazole Sodium?
- RxCUI: 314200 - pantoprazole sodium 40 MG Delayed Release Oral Tablet
- RxCUI: 314200 - pantoprazole 40 MG Delayed Release Oral Tablet
- RxCUI: 314200 - pantoprazole 40 MG (as pantoprazole sodium sesquihydrate 45.1 MG) Delayed Release 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".