NDC 54868-5998 Kapidex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5998 - Kapidex
Product Characteristics
GRAY (C48324 - OPAQUE)
Product Packages
NDC Code 54868-5998-0
Package Description: 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE
NDC Code 54868-5998-1
Package Description: 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product Details
What is NDC 54868-5998?
What are the uses for Kapidex?
Which are Kapidex UNII Codes?
The UNII codes for the active ingredients in this product are:
- DEXLANSOPRAZOLE (UNII: UYE4T5I70X)
- DEXLANSOPRAZOLE (UNII: UYE4T5I70X) (Active Moiety)
Which are Kapidex 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:
- MAGNESIUM CARBONATE (UNII: 0E53J927NA)
- SUCROSE (UNII: C151H8M554)
- HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED (UNII: 2165RE0K14)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- HYPROMELLOSE 2910 (15 CPS) (UNII: 36SFW2JZ0W)
- TALC (UNII: 7SEV7J4R1U)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- CARRAGEENAN (UNII: 5C69YCD2YJ)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- ALUMINUM OXIDE (UNII: LMI26O6933)
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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".