NDC Package 62207-765-60 Fexofenadine Hydrochloride

Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
62207-765-60
Package Description:
8 BLISTER PACK in 1 CARTON / 9 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Fexofenadine Hydrochloride
Non-Proprietary Name:
Fexofenadine Hydrochloride
Substance Name:
Fexofenadine Hydrochloride
Usage Information:
Adults and children 12 years of age and over take one 60 mg tablet with water every 12 hours; do not take more than 2 tablets in 24 hours (for 60 mg) take one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hours (for 180 mg)   children under 12 years of age do not use adults 65 years of age and older ask a doctor consumers with kidney disease ask a doctor
11-Digit NDC Billing Format:
62207076560
NDC to RxNorm Crosswalk:
  • RxCUI: 997420 - fexofenadine HCl 180 MG 24 HR Oral Tablet
  • RxCUI: 997420 - fexofenadine hydrochloride 180 MG Oral Tablet
  • RxCUI: 997501 - fexofenadine HCl 60 MG Oral Tablet
  • RxCUI: 997501 - fexofenadine hydrochloride 60 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Granules India Ltd
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA211075
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-18-2020
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    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
    62207-765-491000 TABLET in 1 BOTTLE
    62207-765-511 BOTTLE in 1 CARTON / 10 TABLET in 1 BOTTLE
    62207-765-885 POUCH in 1 BOX / 10000 TABLET in 1 POUCH

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 62207-765-60?

    The NDC Packaged Code 62207-765-60 is assigned to a package of 8 blister pack in 1 carton / 9 tablet in 1 blister pack of Fexofenadine Hydrochloride, a human over the counter drug labeled by Granules India Ltd. The product's dosage form is tablet and is administered via oral form.

    Is NDC 62207-765 included in the NDC Directory?

    Yes, Fexofenadine Hydrochloride with product code 62207-765 is active and included in the NDC Directory. The product was first marketed by Granules India Ltd on December 18, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 62207-765-60?

    The 11-digit format is 62207076560. 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
    5-3-262207-765-605-4-262207-0765-60