NDC 68788-6915 Glyburide And Metformin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68788 - Preferred Pharmaceuticals Inc.
- 68788-6915 - Glyburide And Metformin Hydrochloride
Product Characteristics
Product Packages
NDC Code 68788-6915-1
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 68788-6915-3
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 68788-6915-6
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 68788-6915-8
Package Description: 120 TABLET in 1 BOTTLE
NDC Code 68788-6915-9
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 68788-6915?
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:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)
- POVIDONE K30 (UNII: U725QWY32X)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
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".