NDC Package 58605-315-16 Maxi-tuss Pe Max

View Billable Units, 11-Digit Format, RxNorm

Package Information
Frequently Asked Questions

Package Information

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

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:

58605-315-16

Package Description:

473 mL in 1 BOTTLE, PLASTIC

Product Code:

58605-315

Proprietary Name:

Maxi-tuss Pe Max

Usage Information:

This product is used as Active Ingredients (in each 5 mL teaspoonful) PurposeGuaifenesin 100 mg Expectorant Phenylephrine HCl 5 mgNasal Decongestant . Temporarily relievesNasal congestion due to the common cold Helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make coughs more productive

11-Digit NDC Billing Format:

58605031516

Billing Unit:

ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

NDC to RxNorm Crosswalk:

473 ML

NDC to RxNorm Crosswalk:

RxCUI: 1358627 - guaiFENesin 100 MG / phenylephrine HCl 5 MG in 5 mL Oral Solution

RxCUI: 1358627 - guaifenesin 20 MG/ML / phenylephrine hydrochloride 1 MG/ML Oral Solution

RxCUI: 1358627 - guaifenesin 100 MG / phenylephrine hydrochloride 5 MG per 5 ML Oral Solution

Labeler Name:

Mcr American Pharmaceuticals, Inc.

Sample Package:

Start Marketing Date:

08-01-2020

Listing Expiration Date:

12-31-2021

Exclude Flag:

Code Structure:

58605 - Mcr American Pharmaceuticals, Inc.
- 58605-315 - Maxi-tuss Pe Max
  - 58605-315-16 - 473 mL in 1 BOTTLE, PLASTIC

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 58605-315-16?

The NDC Packaged Code 58605-315-16 is assigned to a package of 473 ml in 1 bottle, plastic of Maxi-tuss Pe Max, labeled by Mcr American Pharmaceuticals, Inc.. The product's dosage form is and is administered via form.This product is billed per "ML" milliliter and contains an estimated amount of 473 billable units per package.

Is NDC 58605-315 included in the NDC Directory?

No, Maxi-tuss Pe Max with product code 58605-315 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Mcr American Pharmaceuticals, Inc. on August 01, 2020 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 58605-315-16?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 473.

What is the 11-digit format for NDC 58605-315-16?

The 11-digit format is 58605031516. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	58605-315-16	5-4-2	58605-0315-16

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