NDC 43353-338 Pantoprazole Sodium Delayed-release
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43353 - Aphena Pharma Solutions - Tennessee, Llc
- 43353-338 - Pantoprazole Sodium
Product Characteristics
Product Packages
NDC Code 43353-338-09
Package Description: 9000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 43353-338-30
Package Description: 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 43353-338-53
Package Description: 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 43353-338-60
Package Description: 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 43353-338-79
Package Description: 2160 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 43353-338-88
Package Description: 900 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43353-338?
What are the uses for Pantoprazole Sodium Delayed-release?
Which are Pantoprazole Sodium Delayed-release 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 Delayed-release 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)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- MANNITOL (UNII: 3OWL53L36A)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POVIDONE K25 (UNII: K0KQV10C35)
- POVIDONE K90 (UNII: RDH86HJV5Z)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- HYPROMELLOSE 2208 (100 MPA.S) (UNII: B1QE5P712K)
What is the NDC to RxNorm Crosswalk for Pantoprazole Sodium Delayed-release?
- 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
* 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".