NDC Package 58593-275-10 Rompe Pecho DM

Dextromethorphan Hbr,Guaifenesin Liquid Oral - View Billable Units, 11-Digit Format, RxNorm

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:
58593-275-10
Package Description:
10 mL in 1 POUCH
Product Code:
Proprietary Name:
Rompe Pecho DM
Non-Proprietary Name:
Dextromethorphan Hbr, Guaifenesin
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
Uses:temporarily relieves cough as may occur with the common coldhelps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus.
11-Digit NDC Billing Format:
58593027510
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:
Efficient Laboratories Inc
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
10-01-2001
Listing Expiration Date:
12-31-2025
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
58593-275-04118 mL in 1 BOTTLE
58593-275-06178 mL in 1 BOTTLE
58593-275-08237 mL in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 58593-275-10?

The NDC Packaged Code 58593-275-10 is assigned to a package of 10 ml in 1 pouch of Rompe Pecho DM, a human over the counter drug labeled by Efficient Laboratories Inc. The product's dosage form is liquid and is administered via oral form.

Is NDC 58593-275 included in the NDC Directory?

Yes, Rompe Pecho DM with product code 58593-275 is active and included in the NDC Directory. The product was first marketed by Efficient Laboratories Inc on October 01, 2001 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 58593-275-10?

The 11-digit format is 58593027510. 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
5-3-258593-275-105-4-258593-0275-10