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  5. NDC Package Code: 51660-488-69 Loratadine And Pseudoephedrine

NDC Package 51660-488-69 Loratadine And Pseudoephedrine

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
51660-488-69
Package Description:
10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product Code:
51660-488
Proprietary Name:
Loratadine And Pseudoephedrine
Usage Information:
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
11-Digit NDC Billing Format:
51660048869
NDC to RxNorm Crosswalk:
  • 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
    • Labeler Name:
    Ohm Laboratories Inc.
    Sample Package:
    No
    Start Marketing Date:
    11-17-2004
    Listing Expiration Date:
    12-31-2019
    Exclude Flag:
    I
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    51660-488-1515 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51660-488-69?

    The NDC Packaged Code 51660-488-69 is assigned to a package of 10 tablet, extended release in 1 blister pack of Loratadine And Pseudoephedrine, labeled by Ohm Laboratories Inc.. The product's dosage form is and is administered via form.

    Is NDC 51660-488 included in the NDC Directory?

    No, Loratadine And Pseudoephedrine with product code 51660-488 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Ohm Laboratories Inc. on November 17, 2004 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 51660-488-69?

    The 11-digit format is 51660048869. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-251660-488-695-4-251660-0488-69