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  5. NDC Package Code: 65852-009-04 Giltuss Diabetic

NDC Package 65852-009-04 Giltuss Diabetic

Dextromethorphan Hydrobromide,Guaifenesin Solution 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:
65852-009-04
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 118 mL in 1 BOTTLE, PLASTIC
Product Code:
65852-009
Proprietary Name:
Giltuss Diabetic
Non-Proprietary Name:
Dextromethorphan Hydrobromide, Guaifenesin
Substance Name:
Dextromethorphan Hydrochloride; Guaifenesin
Usage Information:
Directions Do not exceed recommended dosageDo not take more than 6 doses in any 24 hours periodKeep dosing cup with productml= mililitersAdults and children 12 years & over 10 ml every 4 hourschildren 6 to under 12 years of age 5 ml every 4 hourschildren 4 to under 6 years of age 2.5 ml every 4 hourschildren under 4 years of age Consult a doctor
11-Digit NDC Billing Format:
65852000904
NDC to RxNorm Crosswalk:
  • RxCUI: 996520 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG in 10 mL Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 10 MG / guaifenesin 100 MG per 5 ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 15 MG / guaifenesin 150 MG per 7.5 ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 20 MG / guaifenesin 200 MG per 10 ML Oral Solution
Product Type:
Human Otc Drug
Labeler Name:
Dextrum Laboratories, Inc
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
10-17-2018
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 65852-009-04?

The NDC Packaged Code 65852-009-04 is assigned to a package of 1 bottle, plastic in 1 carton / 118 ml in 1 bottle, plastic of Giltuss Diabetic, a human over the counter drug labeled by Dextrum Laboratories, Inc. The product's dosage form is solution and is administered via oral form.

Is NDC 65852-009 included in the NDC Directory?

Yes, Giltuss Diabetic with product code 65852-009 is active and included in the NDC Directory. The product was first marketed by Dextrum Laboratories, Inc on October 17, 2018 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 65852-009-04?

The 11-digit format is 65852000904. 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
5-3-265852-009-045-4-265852-0009-04