NDC 33261-830 Glipizideer ER
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33261 - Aidarex Pharmaceuticals Llc
- 33261-830 - Glipizideer
Product Characteristics
Product Packages
NDC Code 33261-830-30
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 33261-830?
What are the uses for Glipizideer ER?
Which are Glipizideer ER UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLIPIZIDE (UNII: X7WDT95N5C)
- GLIPIZIDE (UNII: X7WDT95N5C) (Active Moiety)
Which are Glipizideer ER 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 (2000 MPA.S AT 1%) (UNII: S38J6RZN16)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- SHELLAC (UNII: 46N107B71O)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- AMMONIA (UNII: 5138Q19F1X)
What is the NDC to RxNorm Crosswalk for Glipizideer ER?
- RxCUI: 314006 - glipiZIDE 5 MG 24HR Extended Release Oral Tablet
- RxCUI: 314006 - 24 HR glipizide 5 MG Extended Release Oral Tablet
- RxCUI: 314006 - glipizide ER 5 MG 24 HR Extended Release Oral Tablet
- RxCUI: 314006 - glipizide XL 5 MG 24 HR Extended Release Oral Tablet
- RxCUI: 315107 - glipiZIDE 10 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".