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  5. NDC Package Code: 68599-4785-6 Mckesson Loradatine

NDC Package 68599-4785-6 Mckesson Loradatine

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

Table of Contents

    1. Package Information
    2. 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:
68599-4785-6
Package Description:
50 PACKET in 1 BOX / 1 TABLET in 1 PACKET
Product Code:
68599-4785
Proprietary Name:
Mckesson Loradatine
Non-Proprietary Name:
Loratainde
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:
68599478506
Product Type:
Human Otc Drug
Labeler Name:
Mckesson Medical Surgical
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:
ANDA210722
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
07-01-2025
Listing Expiration Date:
12-31-2026
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.

Frequently Asked Questions

What is NDC 68599-4785-6?

The NDC Packaged Code 68599-4785-6 is assigned to a package of 50 packet in 1 box / 1 tablet in 1 packet of Mckesson Loradatine, a human over the counter drug labeled by Mckesson Medical Surgical. The product's dosage form is tablet and is administered via oral form.

Is NDC 68599-4785 included in the NDC Directory?

Yes, Mckesson Loradatine with product code 68599-4785 is active and included in the NDC Directory. The product was first marketed by Mckesson Medical Surgical on July 01, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 68599-4785-6?

The 11-digit format is 68599478506. 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 5-4-1 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
5-4-168599-4785-65-4-268599-4785-06