NDC 33261-091 Paroxetine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33261 - Aidarex Pharmaceuticals Llc
- 33261-091 - Paroxetine
Product Characteristics
8 MM
ZC;16
Product Packages
NDC Code 33261-091-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
NDC Code 33261-091-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 33261-091?
What are the uses for Paroxetine?
Which are Paroxetine UNII Codes?
The UNII codes for the active ingredients in this product are:
- PAROXETINE HYDROCHLORIDE HEMIHYDRATE (UNII: X2ELS050D8)
- PAROXETINE (UNII: 41VRH5220H) (Active Moiety)
Which are Paroxetine 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 PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- POVIDONES (UNII: FZ989GH94E)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Paroxetine?
- RxCUI: 1738483 - PARoxetine HCl 10 MG Oral Tablet
- RxCUI: 1738483 - paroxetine hydrochloride 10 MG Oral Tablet
- RxCUI: 1738495 - PARoxetine HCl 20 MG Oral Tablet
- RxCUI: 1738495 - paroxetine hydrochloride 20 MG 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".