NDC 63629-8161 Guanfacine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63629 - Bryant Ranch Prepack
- 63629-8161 - Guanfacine
Product Characteristics
Product Packages
NDC Code 63629-8161-1
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 63629-8161?
What are the uses for Guanfacine?
Which are Guanfacine UNII Codes?
The UNII codes for the active ingredients in this product are:
- GUANFACINE HYDROCHLORIDE (UNII: PML56A160O)
- GUANFACINE (UNII: 30OMY4G3MK) (Active Moiety)
Which are Guanfacine 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- FUMARIC ACID (UNII: 88XHZ13131)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
What is the NDC to RxNorm Crosswalk for Guanfacine?
- RxCUI: 862006 - guanFACINE 1 MG 24HR Extended Release Oral Tablet
- RxCUI: 862006 - 24 HR guanfacine 1 MG Extended Release Oral Tablet
- RxCUI: 862006 - guanfacine 1 MG (as guanfacine hydrochloride 1.14 MG) 24 HR Extended Release Oral Tablet
- RxCUI: 862006 - guanfacine 1 MG (as guanfacine hydrochloride 1.15 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".