NDC Package 67296-0385-1 Polymyxin B Sulfate And Trimethoprim

Solution Ophthalmic - 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:
67296-0385-1
Package Description:
10 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Polymyxin B Sulfate And Trimethoprim
Non-Proprietary Name:
Polymyxin B Sulfate And Trimethoprim
Substance Name:
Polymyxin B Sulfate; Trimethoprim Sulfate
Usage Information:
Polymyxin B Sulfate and Trimethoprim Ophthalmic Solution 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, Streptococcus viridans, Haemophilus influenzaeand Pseudomonas aeruginosa.* *Efficacy for this organism in this organ system was studied in fewer than 10 infections.
11-Digit NDC Billing Format:
67296038501
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
Product Type:
Human Prescription Drug
Labeler Name:
Redpharm Drug
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s):
Ophthalmic - Administration to the external eye.
Sample Package:
No
FDA Application Number:
ANDA064211
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
04-16-1998
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.

Frequently Asked Questions

What is NDC 67296-0385-1?

The NDC Packaged Code 67296-0385-1 is assigned to a package of 10 ml in 1 bottle, plastic of Polymyxin B Sulfate And Trimethoprim, a human prescription drug labeled by Redpharm Drug. The product's dosage form is solution and is administered via ophthalmic form.

Is NDC 67296-0385 included in the NDC Directory?

Yes, Polymyxin B Sulfate And Trimethoprim with product code 67296-0385 is active and included in the NDC Directory. The product was first marketed by Redpharm Drug on April 16, 1998 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 67296-0385-1?

The 11-digit format is 67296038501. 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
5-4-167296-0385-15-4-267296-0385-01