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  4. NDC Product Code: 72189-025 Pentoxifylline

NDC 72189-025 Pentoxifylline

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 72189-025?
  5. Pentoxifylline Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72189-025
Proprietary Name:
Pentoxifylline
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Direct_rx
Labeler Code:
72189
Product Label ID:
8f238969-08bb-9464-e053-2995a90abda3
Start Marketing Date: [9]
08-02-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
16 MM
Imprint(s):
APO;033
Score:
1

Product Packages

NDC Code 72189-025-30

Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE

NDC Code 72189-025-60

Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE

NDC Code 72189-025-90

Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE

Product Details

What is NDC 72189-025?

The NDC code 72189-025 is assigned by the FDA to the product Pentoxifylline which is product labeled by Direct_rx. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 72189-025-30 30 tablet, extended release in 1 bottle , 72189-025-60 60 tablet, extended release in 1 bottle , 72189-025-90 90 tablet, extended release 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 Pentoxifylline?

This medication is used to improve the symptoms of a certain blood flow problem in the legs/arms (intermittent claudication due to occlusive artery disease). Pentoxifylline can decrease the muscle aching/pain/cramps during exercise, including walking, that occur with intermittent claudication. Pentoxifylline belongs to a class of drugs known as hemorrheologic agents. It works by helping blood flow more easily through narrowed arteries. This increases the amount of oxygen that can be delivered by the blood when the muscles need more (such as during exercise) thereby increasing walking distance and duration.

Which are Pentoxifylline UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Pentoxifylline 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 Pentoxifylline?

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 code indicates a single concept unique identifier (RXCUI) is associated with this product:
  • RxCUI: 312301 - pentoxifylline 400 MG Extended Release Oral Tablet

* Please review the disclaimer below.

Patient Education

Pentoxifylline


Pentoxifylline is used to improve blood flow in patients with circulation problems to reduce aching, cramping, and tiredness in the hands and feet. It works by decreasing the thickness (viscosity) of blood. This change allows your blood to flow more easily, especially in the small blood vessels of the hands and feet. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
[Learn More]


* 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".