NDC 68788-7230 Glipizide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68788 - Preferred Pharmaceuticals Inc.
- 68788-7230 - Glipizide
Product Characteristics
Product Packages
NDC Code 68788-7230-1
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 68788-7230-3
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 68788-7230-6
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 68788-7230-9
Package Description: 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 68788-7230?
What are the uses for Glipizide?
Which are Glipizide UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLIPIZIDE (UNII: X7WDT95N5C)
- GLIPIZIDE (UNII: X7WDT95N5C) (Active Moiety)
Which are Glipizide 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 LACTOSE (UNII: 3SY5LH9PMK)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CELLULOSE ACETATE (UNII: 3J2P07GVB6)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:2) (UNII: 5KY68S2577)
- CETEARETH-8 (UNII: 4W0XA5SY57)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
What is the NDC to RxNorm Crosswalk for Glipizide?
- RxCUI: 315107 - glipiZIDE 10 MG 24HR Extended Release Oral Tablet
- RxCUI: 315107 - 24 HR glipizide 10 MG Extended Release Oral Tablet
- RxCUI: 315107 - glipizide ER 10 MG 24 HR Extended Release Oral Tablet
- RxCUI: 315107 - glipizide XL 10 MG 24 HR Extended Release 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".