NDC Package 50090-2935-0 Banophen

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:

50090-2935-0

Package Description:

1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE

Product Code:

50090-2935

Proprietary Name:

Banophen

Usage Information:

Take every 4 to 6 hoursdo not take more than 6 doses in 24 hoursuse only with enclosed dosing cup. Do not use with any other devicefind right dose on chart belowmL = milliliteradults and children 12 years and over10-20mL (25 mg to 50 mg)children 6 to under 12 years5-10mL (12.5 mg to 25 mg)children 2 to 5 years of agedo not use unless directed by a doctorchildren under 2 years of agedo not use

11-Digit NDC Billing Format:

50090293500

Billing Unit:

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

NDC to RxNorm Crosswalk:

RxCUI: 1049906 - diphenhydrAMINE HCl 12.5 MG in 5 mL Oral Solution
RxCUI: 1049906 - diphenhydramine hydrochloride 2.5 MG/ML Oral Solution
RxCUI: 1049906 - diphenhydramine HCl 12.5 MG per 5 ML Oral Solution
RxCUI: 1049906 - diphenhydramine hydrochloride 25 MG per 10 ML Oral Solution
RxCUI: 1049906 - diphenhydramine hydrochloride 50 MG per 20 ML Oral Solution

Labeler Name:

A-s Medication Solutions

Sample Package:

FDA Application Number:

part341

Marketing Category:

OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.

Start Marketing Date:

11-20-2006

Listing Expiration Date:

12-31-2022

Exclude Flag:

Code Structure:

50090 - A-s Medication Solutions
- 50090-2935 - Banophen
  - 50090-2935-0 - 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE

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 50090-2935-0?

The NDC Packaged Code 50090-2935-0 is assigned to a package of 1 bottle in 1 carton / 118 ml in 1 bottle of Banophen, labeled by A-s Medication Solutions. The product's dosage form is and is administered via form.

Is NDC 50090-2935 included in the NDC Directory?

No, Banophen with product code 50090-2935 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by A-s Medication Solutions on November 20, 2006 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 50090-2935-0?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 50090-2935-0?

The 11-digit format is 50090293500. 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 5-4-1 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
5-4-1	50090-2935-0	5-4-2	50090-2935-00

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