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  4. NDC Product Code: 54868-5656 Loratadine And Pseudoephedrine

NDC 54868-5656 Loratadine And Pseudoephedrine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 54868-5656?
  5. Loratadine And Pseudoephedrine 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:
54868-5656
Proprietary Name:
Loratadine And Pseudoephedrine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Physicians Total Care, Inc.
Labeler Code:
54868
Product Label ID:
8e73a99c-8fdd-4399-8a7a-d60421209e57
Start Marketing Date: [9]
05-27-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
CAPSULE (C48336)
Size(s):
17 MM
Imprint(s):
RX724
Score:
1

Product Packages

NDC Code 54868-5656-0

Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE

NDC Code 54868-5656-1

Package Description: 2 BLISTER PACK in 1 CARTON / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Code 54868-5656-2

Package Description: 3 BLISTER PACK in 1 CARTON / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Product Details

What is NDC 54868-5656?

The NDC code 54868-5656 is assigned by the FDA to the product Loratadine And Pseudoephedrine which is product labeled by Physicians Total Care, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 54868-5656-0 30 tablet, extended release in 1 bottle , 54868-5656-1 2 blister pack in 1 carton / 5 tablet, extended release in 1 blister pack, 54868-5656-2 3 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 Loratadine And Pseudoephedrine?

Do not divide, crush, chew or dissolve the tabletadults and children 12 years and over: 1 tablet daily with a full glass of water; not more than 1 tablet in 24 hourschildren under 12 years of age: ask a doctorconsumers with liver or kidney disease: ask a doctor

Which are Loratadine And Pseudoephedrine UNII Codes?

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

Which are Loratadine And Pseudoephedrine 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 Loratadine And Pseudoephedrine?

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: 1117562 - pseudoephedrine sulfate 240 MG / loratadine 10 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1117562 - 24 HR loratadine 10 MG / pseudoephedrine sulfate 240 MG Extended Release Oral Tablet
  • RxCUI: 1117562 - loratadine 10 MG / pseudoephedrine sulfate 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".