Loratadine Allergy Relief Tablet
NDC Package 51660-526-30

11-digit billing NDC: 51660052630 · Billing unit: EA · 30 EA per package
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Loratadine Allergy Relief (loratadine) tablets is adults and children 6 years and over1 tablet daily; not more than 1 tablet in 24 hourschildren under 6 years of ageask a doctorconsumers with liver or kidney diseaseask a doctor. This formulation utilizes a tablet delivery system. Marketed by Ohm Laboratories Inc., this product is identified by NDC 51660-526 and is authorized under FDA application ANDA076134.

Identification & Billing

NDC Package Code
51660-526-30
Package Description
30 TABLET in 1 BOTTLE
Product Code
51660-526
11-Digit Billing Format
51660052630
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
30 EA
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Loratadine Allergy Relief
Non-Proprietary Name
Loratadine
Substance Name
Loratadine
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
Adults and children 6 years and over1 tablet daily; not more than 1 tablet in 24 hourschildren under 6 years of ageask a doctorconsumers with liver or kidney diseaseask a doctor

Regulatory & Marketing

Labeler Name
Ohm Laboratories Inc.
Product Type
Human Otc Drug
FDA Application #
ANDA076134
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
11-01-2017
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (51660-526). Click a package code to view its specific billing and regulatory data.

51660-526-01
100 TABLET in 1 BOTTLE
51660-526-03
5000 TABLET in 1 BAG
51660-526-05
500 TABLET in 1 BOTTLE
51660-526-11
10 TABLET in 1 BLISTER PACK
51660-526-31
30 TABLET in 1 BLISTER PACK
51660-526-53
300 TABLET in 1 BOTTLE

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 51660-526-30 identifies a specific commercial package of 30 tablet in 1 bottle of Loratadine Allergy Relief, a human over the counter drug labeled by Ohm Laboratories Inc.. This tablet is formulated for oral use and contains loratadine as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Ohm Laboratories Inc. on November 01, 2017. The current certification is valid through December 31, 2026.

How is this Ohm Laboratories Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51660052630. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 30 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
51660-526-30
11-Digit CMS (5-4-2)
51660-0526-30

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.