NDC 54868-4965 Avandamet
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4965 - Avandamet
Product Characteristics
Product Packages
NDC Code 54868-4965-0
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-4965-1
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-4965-2
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 54868-4965?
What are the uses for Avandamet?
Which are Avandamet UNII Codes?
The UNII codes for the active ingredients in this product are:
- ROSIGLITAZONE MALEATE (UNII: KX2339DP44)
- ROSIGLITAZONE (UNII: 05V02F2KDG) (Active Moiety)
- METFORMIN HYDROCHLORIDE (UNII: 786Z46389E)
- METFORMIN (UNII: 9100L32L2N) (Active Moiety)
Which are Avandamet 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:
- HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POVIDONE K29/32 (UNII: 390RMW2PEQ)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Avandamet?
- RxCUI: 861760 - rosiglitazone maleate 2 MG / metFORMIN HCl 1000 MG Oral Tablet
- RxCUI: 861760 - metformin hydrochloride 1000 MG / rosiglitazone 2 MG Oral Tablet
- RxCUI: 861760 - metformin hydrochloride 1000 MG / rosiglitazone (as rosiglitazone maleate) 2 MG Oral Tablet
- RxCUI: 861762 - Avandamet 2 MG / 1000 MG Oral Tablet
- RxCUI: 861762 - metformin hydrochloride 1000 MG / rosiglitazone 2 MG Oral Tablet [Avandamet]
* 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".