1. Home
  2. Labeler Index
  3. Aurohealth Llc
  4. 58602-702
  5. NDC Package Code: 58602-702-09 Loratadine

NDC Package 58602-702-09 Loratadine

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

Table of Contents

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

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:
58602-702-09
Package Description:
1 BOTTLE in 1 CARTON / 30 TABLET in 1 BOTTLE
Product Code:
58602-702
Proprietary Name:
Loratadine
Non-Proprietary Name:
Loratadine
Substance Name:
Loratadine
Usage Information:
This medication is an antihistamine that treats symptoms such as itching, runny nose, watery eyes, and sneezing from "hay fever" and other allergies. It is also used to relieve itching from hives. Loratadine does not prevent hives or prevent/treat a serious allergic reaction (anaphylaxis). Therefore, if your doctor has prescribed epinephrine to treat allergic reactions, always carry your epinephrine injector with you. Do not use loratadine in place of your epinephrine. If you are self-treating with this medication, it is important to read the manufacturer's package instructions carefully so you know when to consult your doctor or pharmacist. (See also Precautions section.) If you are using the tablets or capsules, do not use in children younger than 6 years unless directed by the doctor. If you are using the liquid or chewable tablets, do not use in children younger than 2 years unless directed by the doctor.
11-Digit NDC Billing Format:
58602070209
NDC to RxNorm Crosswalk:
  • RxCUI: 311372 - loratadine 10 MG 24HR Oral Tablet
  • RxCUI: 311372 - loratadine 10 MG Oral Tablet
  • RxCUI: 311372 - loratadine 10 MG 24 HR Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Aurohealth Llc
    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.
    • Active Ingredient(s):
  • LORATADINE 10 mg/1
    • Sample Package:
    No
    FDA Application Number:
    ANDA208314
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-16-2018
    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
    58602-702-0410 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
    58602-702-055 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
    58602-702-151 BOTTLE in 1 CARTON / 60 TABLET in 1 BOTTLE
    58602-702-171 BOTTLE in 1 CARTON / 45 TABLET in 1 BOTTLE
    58602-702-191 BOTTLE in 1 CARTON / 90 TABLET in 1 BOTTLE
    58602-702-211 BOTTLE in 1 CARTON / 100 TABLET in 1 BOTTLE
    58602-702-231 BOTTLE in 1 CARTON / 120 TABLET in 1 BOTTLE
    58602-702-291 BOTTLE in 1 CARTON / 150 TABLET in 1 BOTTLE
    58602-702-321 BOTTLE in 1 CARTON / 180 TABLET in 1 BOTTLE
    58602-702-381 BOTTLE in 1 CARTON / 300 TABLET in 1 BOTTLE
    58602-702-391 BOTTLE in 1 CARTON / 365 TABLET in 1 BOTTLE
    58602-702-401 BOTTLE in 1 CARTON / 500 TABLET in 1 BOTTLE
    58602-702-441 BOTTLE in 1 CARTON / 400 TABLET in 1 BOTTLE
    58602-702-541 BOTTLE in 1 CARTON / 70 TABLET in 1 BOTTLE
    58602-702-601 BLISTER PACK in 1 CARTON / 5 TABLET in 1 BLISTER PACK
    58602-702-672 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
    58602-702-811 BOTTLE in 1 CARTON / 108 TABLET in 1 BOTTLE
    58602-702-831 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
    58602-702-843 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 58602-702-09?

    The NDC Packaged Code 58602-702-09 is assigned to a package of 1 bottle in 1 carton / 30 tablet in 1 bottle of Loratadine, a human over the counter drug labeled by Aurohealth Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 58602-702 included in the NDC Directory?

    Yes, Loratadine with product code 58602-702 is active and included in the NDC Directory. The product was first marketed by Aurohealth Llc on April 16, 2018 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 58602-702-09?

    The 11-digit format is 58602070209. 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
    5-3-258602-702-095-4-258602-0702-09