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  4. NDC Product Code: 16590-181 Paroxetine

NDC 16590-181 Paroxetine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 16590-181?
  5. Paroxetine Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
16590-181
Proprietary Name:
Paroxetine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Stat Rx Usa Llc
Labeler Code:
16590
Product Label ID:
42646d8c-2c00-4575-b215-bad0789a1ce0
Start Marketing Date: [9]
07-25-2007
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
Shape:
CAPSULE (C48336)
Size(s):
10 MM
Imprint(s):
56;C
Score:
2

Code Structure Chart

Product Details

What is NDC 16590-181?

The NDC code 16590-181 is assigned by the FDA to the product Paroxetine which is product labeled by Stat Rx Usa Llc. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 16590-181-15 15 tablet, film coated in 1 bottle , 16590-181-28 28 tablet, film coated in 1 bottle , 16590-181-30 30 tablet, film coated in 1 bottle , 16590-181-60 60 tablet, film coated in 1 bottle , 16590-181-90 90 tablet, film coated in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Paroxetine?

The use of MAOIs intended to treat depression with, or within 14 days of treatment with, paroxetine tablets is contraindicated (see WARNINGS). Do not start paroxetine tablets in a patient who is being treated with a reversible MAOI such as linezolid or methylene blue because of an increased risk of serotonin syndrome or neuroleptic malignant syndrome (NMS)-like reactions (see WARNINGS). Concomitant use with thioridazine is contraindicated (see WARNINGS and PRECAUTIONS). Concomitant use in patients taking pimozide is contraindicated (see PRECAUTIONS).  Paroxetine tablets are contraindicated in patients with a hypersensitivity to paroxetine or any of the inactive ingredients in paroxetine tablets.

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:

What is the NDC to RxNorm Crosswalk for Paroxetine?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

Product Footnotes

[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".