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  5. NDC Package Code: 50419-788-01 Cipro

NDC Package 50419-788-01 Cipro

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
50419-788-01
Package Description:
50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code:
50419-788
Proprietary Name:
Cipro
Usage Information:
This medication is used to treat a variety of bacterial infections. Ciprofloxacin belongs to a class of drugs called quinolone antibiotics. It works by stopping the growth of bacteria. This antibiotic treats only bacterial infections. It will not work for virus infections (such as common cold, flu). Using any antibiotic when it is not needed can cause it to not work for future infections.
11-Digit NDC Billing Format:
50419078801
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
50 EA
Labeler Name:
Bayer Healthcare Pharmaceuticals Inc.
Sample Package:
No
FDA Application Number:
NDA021473
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
10-01-2012
End Marketing Date:
07-27-2016
Listing Expiration Date:
07-27-2016
Exclude Flag:
D
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
50419-788-0038220 TABLET, FILM COATED, EXTENDED RELEASE in 1 DRUM

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 50419-788-01?

The NDC Packaged Code 50419-788-01 is assigned to a package of 50 tablet, film coated, extended release in 1 bottle, plastic of Cipro, labeled by Bayer Healthcare Pharmaceuticals Inc.. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 50 billable units per package.

Is NDC 50419-788 included in the NDC Directory?

No, Cipro with product code 50419-788 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Bayer Healthcare Pharmaceuticals Inc. on October 01, 2012 and its listing in the NDC Directory is set to expire on July 27, 2016 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 50419-788-01?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 50.

What is the 11-digit format for NDC 50419-788-01?

The 11-digit format is 50419078801. 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
5-3-250419-788-015-4-250419-0788-01