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  4. NDC Product Code: 67046-219 Furosemide

NDC 67046-219 Furosemide

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 67046-219?
  5. Furosemide 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:
67046-219
Proprietary Name:
Furosemide
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Contract Pharmacy Services-pa
Labeler Code:
67046
Product Label ID:
5a95bc6e-5cee-4813-e053-2a91aa0a8c35
Start Marketing Date: [9]
10-02-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
8 MM
Imprint(s):
MYLAN;216;40
Score:
2

Product Packages

NDC Code 67046-219-07

Package Description: 7 TABLET in 1 BLISTER PACK

NDC Code 67046-219-14

Package Description: 14 TABLET in 1 BLISTER PACK

NDC Code 67046-219-15

Package Description: 15 TABLET in 1 BLISTER PACK

NDC Code 67046-219-20

Package Description: 20 TABLET in 1 BLISTER PACK

NDC Code 67046-219-21

Package Description: 21 TABLET in 1 BLISTER PACK

NDC Code 67046-219-28

Package Description: 28 TABLET in 1 BLISTER PACK

NDC Code 67046-219-30

Package Description: 30 TABLET in 1 BLISTER PACK

NDC Code 67046-219-60

Package Description: 60 TABLET in 1 BLISTER PACK

Product Details

What is NDC 67046-219?

The NDC code 67046-219 is assigned by the FDA to the product Furosemide which is product labeled by Contract Pharmacy Services-pa. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 67046-219-07 7 tablet in 1 blister pack , 67046-219-14 14 tablet in 1 blister pack , 67046-219-15 15 tablet in 1 blister pack , 67046-219-20 20 tablet in 1 blister pack , 67046-219-21 21 tablet in 1 blister pack , 67046-219-28 28 tablet in 1 blister pack , 67046-219-30 30 tablet in 1 blister pack , 67046-219-60 60 tablet in 1 blister pack . 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 Furosemide?

Furosemide is used to reduce extra fluid in the body (edema) caused by conditions such as heart failure, liver disease, and kidney disease. This can lessen symptoms such as shortness of breath and swelling in your arms, legs, and abdomen. This drug is also used to treat high blood pressure. Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. Furosemide is a "water pill" (diuretic) that causes you to make more urine. This helps your body get rid of extra water and salt.

Which are Furosemide UNII Codes?

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

Which are Furosemide 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 Furosemide?

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".