NDC 67544-511 Glyburide And Metformin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 67544-511?
What are the uses for Glyburide And Metformin Hydrochloride?
Which are Glyburide And 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 And 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SORBIC ACID (UNII: X045WJ989B)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:2) (UNII: 5KY68S2577)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Glyburide And Metformin Hydrochloride?
- 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
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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".