NDC 54868-5840 Januvia
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5840 - Januvia
Product Characteristics
BROWN (C48332 - BEIGE)
10 MM
277
Product Packages
NDC Code 54868-5840-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-5840-1
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-5840?
What are the uses for Januvia?
Which are Januvia UNII Codes?
The UNII codes for the active ingredients in this product are:
- SITAGLIPTIN PHOSPHATE (UNII: TS63EW8X6F)
- SITAGLIPTIN (UNII: QFP0P1DV7Z) (Active Moiety)
Which are Januvia 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:
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Januvia?
- RxCUI: 665033 - SITagliptin 100 MG Oral Tablet
- RxCUI: 665033 - sitagliptin 100 MG Oral Tablet
- RxCUI: 665033 - sitagliptin 100 MG (as sitagliptin phosphate monohydrate 128.5 MG) Oral Tablet
- RxCUI: 665036 - Januvia 100 MG Oral Tablet
- RxCUI: 665036 - sitagliptin 100 MG Oral Tablet [Januvia]
* 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".