Diabetic Tussin Nighttime Cold And Flu
NDC Package 61787-516-04

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Diabetic Tussin Nighttime Cold And Flu is •take every 4 to 6 hours•do not exceed more than 6 doses in 24 hours for adults and children over 12 years of ageAdults10 mL (2 teaspoons)Children under 12 yearsask a doctor. Marketed by Medtech Products Inc, this product is identified by NDC 61787-516 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
61787-516-04
Package Description
1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Product Code
61787-516
11-Digit Billing Format
61787051604
RxNorm Crosswalk
  • RxCUI: 1094131 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / diphenhydrAMINE HCl 12.5 MG in 5 mL Oral Solution
  • RxCUI: 1094131 - acetaminophen 65 MG/ML / dextromethorphan hydrobromide 2 MG/ML / diphenhydramine hydrochloride 2.5 MG/ML Oral Solution
  • RxCUI: 1094131 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / diphenhydramine hydrochloride 12.5 MG per 5 ML Oral Solution
  • RxCUI: 1094131 - APAP 65 MG/ML / Dextromethorphan Hydrobromide 2 MG/ML / Diphenhydramine Hydrochloride 2.5 MG/ML Oral Solution

Clinical Specifications

Proprietary Name
Diabetic Tussin Nighttime Cold And Flu
Dosage Form
-
Usage Information
•take every 4 to 6 hours•do not exceed more than 6 doses in 24 hours for adults and children over 12 years of ageAdults10 mL (2 teaspoons)Children under 12 yearsask a doctor

Regulatory & Marketing

Labeler Name
Medtech Products Inc
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
02-01-2020
Listing Expiration
12-31-2024
Exclude Flag
I
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 61787-516-04 identifies a specific commercial package of 1 bottle in 1 carton / 118 ml in 1 bottle of Diabetic Tussin Nighttime Cold And Flu, labeled by Medtech Products Inc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Medtech Products Inc on February 01, 2020. The current certification is valid through December 31, 2024.

How is this Medtech Products Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 61787051604. 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)
61787-516-04
11-Digit CMS (5-4-2)
61787-0516-04

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