NDC 53808-0935 Pantoprazole Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 53808-0935?
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:
- CALCIUM STEARATE (UNII: 776XM7047L)
- CROSPOVIDONE (UNII: 68401960MK)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82)
- MANNITOL (UNII: 3OWL53L36A)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Pantoprazole Sodium?
- RxCUI: 251872 - pantoprazole sodium 20 MG Delayed Release Oral Tablet
- RxCUI: 251872 - pantoprazole 20 MG Delayed Release Oral Tablet
- RxCUI: 251872 - pantoprazole 20 MG (as pantoprazole sodium sesquihydrate 22.56 MG) Delayed Release Oral Tablet
- RxCUI: 314200 - pantoprazole sodium 40 MG Delayed Release Oral Tablet
- RxCUI: 314200 - pantoprazole 40 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".