Loperamide Hcl And Simethicone Tablet
NDC Package 51660-069-06

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Loperamide Hcl And Simethicone tablets is •drink plenty of clear fluids to help prevent dehydration caused by diarrhea•take only on an empty stomach (1 hour before or 2 hours after a meal)•take with a full (8 oz.) glass of water•find right dose on chart below. This formulation utilizes a tablet delivery system. Marketed by Ohm Laboratories Inc., this product is identified by NDC 51660-069 and is authorized under FDA application ANDA077500.

Identification & Billing

NDC Package Code
51660-069-06
Package Description
6 TABLET in 1 BLISTER PACK
Product Code
51660-069
11-Digit Billing Format
51660006906
RxNorm Crosswalk
  • RxCUI: 978001 - loperamide HCl 2 MG / simethicone 125 MG Oral Tablet
  • RxCUI: 978001 - loperamide hydrochloride 2 MG / simethicone 125 MG Oral Tablet

Clinical Specifications

Proprietary Name
Loperamide Hcl And Simethicone
Non-Proprietary Name
Loperamide Hcl And Simethicone
Substance Name
Dimethicone; Loperamide Hydrochloride
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)
Pharmacologic Class
Usage Information
•drink plenty of clear fluids to help prevent dehydration caused by diarrhea•take only on an empty stomach (1 hour before or 2 hours after a meal)•take with a full (8 oz.) glass of water•find right dose on chart below. If possible, use weight to dose; otherwise, use age.adults and children 12 years and over2 caplets after the first loosestool; 1 caplet after eachsubsequent loose stool;but no more than 4 caplets in 24 hourschildren 9-11 years (60-95 lbs)1 caplet after the first loosestool; 1/2 caplet after eachsubsequent loose stool;but no more than 3 caplets in 24 hourschildren 6-8 years (48-59 lbs)1 caplet after the first loosestool; 1/2 caplet after eachsubsequent loose stool;but no more than 2 caplets in 24 hourschildren 2-5 years (34 to 47 lbs)ask a doctorchildren under 2 years (upto 33 lbs)do not use

Regulatory & Marketing

Labeler Name
Ohm Laboratories Inc.
Product Type
Human Otc Drug
FDA Application #
ANDA077500
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
01-13-2022
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 (51660-069). Click a package code to view its specific billing and regulatory data.

51660-069-12
2 BLISTER PACK in 1 CARTON / 6 TABLET in 1 BLISTER PACK
51660-069-18
3 BLISTER PACK in 1 CARTON / 6 TABLET in 1 BLISTER PACK
51660-069-24
4 BLISTER PACK in 1 CARTON / 6 TABLET in 1 BLISTER PACK

* 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 51660-069-06 identifies a specific commercial package of 6 tablet in 1 blister pack of Loperamide Hcl And Simethicone, a human over the counter drug labeled by Ohm Laboratories Inc.. This tablet is formulated for oral use and contains dimethicone; loperamide hydrochloride 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 January 13, 2022. 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: 51660006906. 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)
51660-069-06
11-Digit CMS (5-4-2)
51660-0069-06

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