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  4. NDC Product Code: 21130-557 Fexofenadine Hcl And Pseudoephedrine Hci

NDC 21130-557 Fexofenadine Hcl And Pseudoephedrine Hci

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 21130-557?
  5. Fexofenadine Hcl And Pseudoephedrine Hci 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:
21130-557
Proprietary Name:
Fexofenadine Hcl And Pseudoephedrine Hci
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Safeway Inc
Labeler Code:
21130
Product Label ID:
65a92250-d0e8-c902-b14c-67f53ab26635
Start Marketing Date: [9]
02-05-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
CAPSULE (C48336)
Size(s):
21 MM
Imprint(s):
RDY;572
Score:
1

Code Structure Chart

Product Details

What is NDC 21130-557?

The NDC code 21130-557 is assigned by the FDA to the product Fexofenadine Hcl And Pseudoephedrine Hci which is product labeled by Safeway Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 21130-557-35 2 blister pack in 1 carton / 5 tablet, extended release 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 Fexofenadine Hcl And Pseudoephedrine Hci?

Do not divide, crush, chew or dissolve the tablet; swallow tablet wholeadults and children 12 years of age and over   take 1 tablet with a glass of water every 24 hours on an empty stomach; 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 Hcl And Pseudoephedrine Hci UNII Codes?

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

Which are Fexofenadine Hcl And Pseudoephedrine Hci 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 Hcl And Pseudoephedrine Hci?

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:
  • RxCUI: 997415 - fexofenadine HCl 180 MG / pseudoephedrine HCl 240 MG 24HR Extended Release Oral Tablet
  • RxCUI: 997415 - 24 HR fexofenadine hydrochloride 180 MG / pseudoephedrine hydrochloride 240 MG Extended Release Oral Tablet
  • RxCUI: 997415 - fexofenadine hydrochloride 180 MG / pseudoephedrine hydrochloride 240 MG 24 HR Extended Release Oral Tablet

* 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".