NDC 54868-5364 Glipizide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5364 - Glipizide
Product Characteristics
Product Packages
NDC Code 54868-5364-0
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-5364-1
Package Description: 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-5364-2
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 54868-5364?
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:
- ACETYLTRIBUTYL CITRATE (UNII: 0ZBX0N59RZ)
- HYDROXYETHYL CELLULOSE (140 CPS AT 5%) (UNII: 8136Y38GY5)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Glipizide?
- RxCUI: 310489 - glipiZIDE 2.5 MG 24HR Extended Release Oral Tablet
- RxCUI: 310489 - 24 HR glipizide 2.5 MG Extended Release Oral Tablet
- RxCUI: 310489 - glipizide ER 2.5 MG 24 HR Extended Release Oral Tablet
- RxCUI: 310489 - glipizide XL 2.5 MG 24 HR Extended Release Oral Tablet
- RxCUI: 314006 - glipiZIDE 5 MG 24HR 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".