NDC 43353-609 Buspirone Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43353 - Aphena Pharma Solutions - Tennessee, Llc
- 43353-609 - Buspirone Hydrochloride
Product Characteristics
Product Packages
NDC Code 43353-609-53
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-609-60
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-609-80
Package Description: 180 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43353-609?
What are the uses for Buspirone Hydrochloride?
Which are Buspirone Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- BUSPIRONE HYDROCHLORIDE (UNII: 207LT9J9OC)
- BUSPIRONE (UNII: TK65WKS8HL) (Active Moiety)
Which are Buspirone Hydrochloride 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Buspirone Hydrochloride?
- RxCUI: 866018 - busPIRone HCl 15 MG Oral Tablet
- RxCUI: 866018 - buspirone hydrochloride 15 MG Oral Tablet
- RxCUI: 866018 - buspirone hydrochloride 15 MG (buspirone 13.7 MG) Oral Tablet
- RxCUI: 866083 - busPIRone HCl 10 MG Oral Tablet
- RxCUI: 866083 - buspirone hydrochloride 10 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Buspirone
Buspirone is used to treat anxiety disorders or in the short-term treatment of symptoms of anxiety. Buspirone is in a class of medications called anxiolytics. It works by changing the amounts of certain natural substances in the brain.
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* 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".