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  4. NDC Product Code: 54868-0159 Probenecid

NDC 54868-0159 Probenecid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 54868-0159?
  5. Probenecid 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:
54868-0159
Proprietary Name:
Probenecid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Physicians Total Care, Inc.
Labeler Code:
54868
Product Label ID:
9eeedc83-f6cc-4383-83ec-d7992a96b7b4
Start Marketing Date: [9]
03-28-1995
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
OVAL (C48345)
Size(s):
18 MM
Imprint(s):
DAN;DAN;5347
Score:
2

Product Packages

NDC Code 54868-0159-0

Package Description: 60 TABLET, FILM COATED in 1 BOTTLE

NDC Code 54868-0159-2

Package Description: 100 TABLET, FILM COATED in 1 BOTTLE

NDC Code 54868-0159-3

Package Description: 30 TABLET, FILM COATED in 1 BOTTLE

NDC Code 54868-0159-4

Package Description: 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Code 54868-0159-5

Package Description: 180 TABLET, FILM COATED in 1 BOTTLE

Product Details

What is NDC 54868-0159?

The NDC code 54868-0159 is assigned by the FDA to the product Probenecid which is product labeled by Physicians Total Care, Inc.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 54868-0159-0 60 tablet, film coated in 1 bottle , 54868-0159-2 100 tablet, film coated in 1 bottle , 54868-0159-3 30 tablet, film coated in 1 bottle , 54868-0159-4 10 tablet, film coated in 1 bottle, plastic , 54868-0159-5 180 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 Probenecid?

This medication is used to prevent gout and gouty arthritis. It will not treat a sudden/severe attack of gout and may make it worse. Probenecid belongs to a class of drugs known as uricosurics. It lowers high levels of uric acid in your body by helping the kidneys to get rid of uric acid. When uric acid levels get too high, crystals can form in the joints, causing gout. Lowering uric acid levels may also help your kidneys. Probenecid may be prescribed in combination with certain antibiotics (such as penicillins). It increases the levels of antibiotic in the blood, which helps the antibiotic work better. Probenecid should not be used in children younger than 2 years.

Which are Probenecid UNII Codes?

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

Which are Probenecid 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 Probenecid?

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:

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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".