NDC 59547-210 Glycate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 59547-210?
What are the uses for Glycate?
Which are Glycate UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCOPYRROLATE (UNII: V92SO9WP2I)
- GLYCOPYRRONIUM (UNII: A14FB57V1D) (Active Moiety)
Which are Glycate 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 PYROPHOSPHATE (UNII: X69NU20D19)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONES (UNII: FZ989GH94E)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Glycate?
- RxCUI: 1247658 - glycopyrrolate 1.5 MG Oral Tablet
- RxCUI: 1437975 - Glycate 1.5 MG Oral Tablet
- RxCUI: 1437975 - glycopyrrolate 1.5 MG Oral Tablet [Glycate]
* 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".