NDC 50090-5991 Guanfacine Extended-release
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-5991 - Guanfacine
Product Characteristics
Product Packages
NDC Code 50090-5991-0
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 50090-5991?
What are the uses for Guanfacine Extended-release?
Which are Guanfacine Extended-release 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 Extended-release 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:
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- POLYVINYL ACETATE PHTHALATE (UNII: 58QVG85GW3)
- POVIDONE K12 (UNII: 333AG72FWJ)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Guanfacine Extended-release?
- RxCUI: 862019 - guanFACINE 3 MG 24HR Extended Release Oral Tablet
- RxCUI: 862019 - 24 HR guanfacine 3 MG Extended Release Oral Tablet
- RxCUI: 862019 - guanfacine 3 MG (as guanfacine hydrochloride 3.42 MG) 24 HR Extended Release Oral Tablet
- RxCUI: 862019 - guanfacine 3 MG (as guanfacine hydrochloride 3.45 MG) 24 HR Extended Release Oral Tablet
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[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".