NDC 55648-434 Pantoprazole Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55648 - Wockhardt Limited
- 55648-434 - Pantoprazole Sodium
Product Characteristics
12 MM
W434
Product Packages
NDC Code 55648-434-01
Package Description: 30 TABLET, DELAYED RELEASE in 1 BOTTLE
NDC Code 55648-434-02
Package Description: 1000 TABLET, DELAYED RELEASE in 1 BOTTLE
NDC Code 55648-434-03
Package Description: 100 BLISTER PACK in 1 CARTON / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
NDC Code 55648-434-04
Package Description: 90 TABLET, DELAYED RELEASE in 1 BOTTLE
NDC Code 55648-434-05
Package Description: 100 TABLET, DELAYED RELEASE in 1 BOTTLE
Product Details
What is NDC 55648-434?
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:
- MANNITOL (UNII: 3OWL53L36A)
- STARCH, CORN (UNII: O8232NY3SJ)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- CALCIUM STEARATE (UNII: 776XM7047L)
- TALC (UNII: 7SEV7J4R1U)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- SHELLAC (UNII: 46N107B71O)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
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
* 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".