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  4. NDC Product Code: 68554-5061 Fexofenadine Hydrochloride

NDC 68554-5061 Fexofenadine Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 68554-5061?
  5. Fexofenadine Hydrochloride 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:
68554-5061
Proprietary Name:
Fexofenadine Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hetero Labs Limited
Labeler Code:
68554
Product Label ID:
412af925-12e9-405f-b3c3-d5c3d0b5d5c2
Start Marketing Date: [9]
08-23-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
Shape:
ROUND (C48348)
Size(s):
6 MM
Imprint(s):
J;42
Score:
1

Code Structure Chart

Product Details

What is NDC 68554-5061?

The NDC code 68554-5061 is assigned by the FDA to the product Fexofenadine Hydrochloride which is product labeled by Hetero Labs Limited. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 68554-5061-0 1 bottle in 1 carton / 30 tablet, film coated in 1 bottle, 68554-5061-1 1 bottle in 1 carton / 100 tablet, film coated in 1 bottle, 68554-5061-2 1 bottle in 1 carton / 500 tablet, film coated in 1 bottle, 68554-5061-5 10 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack (68554-5061-4), 68554-5061-6 22 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack (68554-5061-3). 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 Fexofenadine Hydrochloride?

30 mgadults and children 12 years of age and overtake two 30 mg tablets with water every 12 hours; do not take more than 4 tablets in        24 hourschildren 6 to under 12 years of agetake one 30 mg tablet with water every 12 hours; do not take more than 2 tablets in              24 hourschildren under 6 years of agedo not useadults 65 years of age and olderask a doctorconsumers with kidney diseaseask a doctor60 mgadults and children 12 years of age and overtake one 60 mg tablet with water every 12 hours; do not take more than 2 tablets in       24 hourschildren under 12 years of agedo not useadults 65 years of age and olderask a doctorconsumers with kidney diseaseask a doctor180 mgadults and children 12 years of age and overtake one 180 mg tablet with water once a day; do not take more than 1 tablet in              24 hourschildren under 12 years of agedo not useadults 65 years of age and olderask a doctorconsumers with kidney diseaseask a doctor

Which are Fexofenadine Hydrochloride UNII Codes?

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

Which are Fexofenadine Hydrochloride 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 Fexofenadine Hydrochloride?

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:

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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".