NDC 10544-580 Glyburide-metformin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10544 - Blenheim Pharmacal, Inc.
- 10544-580 - Glyburide-metformin Hydrochloride
Product Characteristics
Product Packages
NDC Code 10544-580-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 10544-580-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 10544-580?
What are the uses for Glyburide-metformin Hydrochloride?
Which are Glyburide-metformin Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYBURIDE (UNII: SX6K58TVWC)
- GLYBURIDE (UNII: SX6K58TVWC) (Active Moiety)
- METFORMIN HYDROCHLORIDE (UNII: 786Z46389E)
- METFORMIN (UNII: 9100L32L2N) (Active Moiety)
Which are Glyburide-metformin Hydrochloride 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:
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- POVIDONE (UNII: FZ989GH94E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- PROPYLENE GLYCOL, (R)- (UNII: 602HN5L69H)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Glyburide-metformin Hydrochloride?
- RxCUI: 861748 - glyBURIDE 2.5 MG / metFORMIN HCl 500 MG Oral Tablet
- RxCUI: 861748 - glyburide 2.5 MG / metformin hydrochloride 500 MG Oral Tablet
- RxCUI: 861753 - glyBURIDE 5 MG / metFORMIN HCl 500 MG Oral Tablet
- RxCUI: 861753 - glyburide 5 MG / metformin hydrochloride 500 MG Oral Tablet
- RxCUI: 861753 - glyburide 5 MG / metformin HCl 500 MG 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".