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  5. NDC Package Code: 67296-0850-1 Polymyxin B Sulfate And Trimethoprim Sulfate

NDC Package 67296-0850-1 Polymyxin B Sulfate And Trimethoprim Sulfate

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

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:
67296-0850-1
Package Description:
10 mL in 1 BOTTLE
Product Code:
67296-0850
Proprietary Name:
Polymyxin B Sulfate And Trimethoprim Sulfate
Usage Information:
Polymyxin B sulfate and trimethoprim ophthalmic solution, USP is indicated in the treatment of surface ocular bacterial infections, including acute bacterial conjunctivitis, and blepharoconjunctivitis, caused by susceptible strains of the following microorganisms: Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pneumoniae, Streptococcusviridans,Haemophilusinfluenzae andPseudomonas aeruginosa.**Efficacy for this organism in this organ system was studied in fewer than 10 infections.
11-Digit NDC Billing Format:
67296085001
NDC to RxNorm Crosswalk:
  • RxCUI: 244967 - polymyxin B sulfate 10,000 UNT / trimethoprim sulfate 1 MG in ML Ophthalmic Solution
  • RxCUI: 244967 - polymyxin B 10000 UNT/ML / trimethoprim 1 MG/ML Ophthalmic Solution
  • RxCUI: 244967 - polymyxin B 10,000 UNT / trimethoprim (as trimethoprim sulfate) 0.1 % Ophthalmic Solution
  • RxCUI: 244967 - polymyxin B 10,000 UNT / trimethoprim 0.1 % Ophthalmic Solution
  • RxCUI: 244967 - Polymyxin B 10000 UNT/ML / TMP 1 MG/ML Ophthalmic Solution
Labeler Name:
Redpharm Drug
Sample Package:
No
FDA Application Number:
NDA050567
Marketing Category:
NDA AUTHORIZED GENERIC - A product marketed as a "generic" drug under an approved New Drug Application (NDA), rather than an Abbreviated New Drug Application (ANDA),.
Start Marketing Date:
04-29-1997
Listing Expiration Date:
12-31-2025
Exclude Flag:
E
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 67296-0850-1?

The NDC Packaged Code 67296-0850-1 is assigned to a package of 10 ml in 1 bottle of Polymyxin B Sulfate And Trimethoprim Sulfate, labeled by Redpharm Drug. The product's dosage form is and is administered via form.

Is NDC 67296-0850 included in the NDC Directory?

No, Polymyxin B Sulfate And Trimethoprim Sulfate with product code 67296-0850 is excluded from the NDC Directory for failure to respond to FDA's requests for correction to deficient or non-compliant submissions. The product was first marketed by Redpharm Drug on April 29, 1997 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 67296-0850-1?

The 11-digit format is 67296085001. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-167296-0850-15-4-267296-0850-01