NDC Package 67296-0661-1 Bacitracin Zinc And Polymyxin B Sulfate

Ointment 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:
67296-0661-1
Package Description:
1 TUBE in 1 CARTON / 3.5 g in 1 TUBE
Product Code:
Proprietary Name:
Bacitracin Zinc And Polymyxin B Sulfate
Non-Proprietary Name:
Bacitracin Zinc And Polymyxin B Sulfate
Substance Name:
Bacitracin Zinc; Polymyxin B Sulfate
Usage Information:
For the treatment of superficial ocular infections involving the conjunctiva and/or cornea caused by organisms susceptible to bacitracin zinc and polymyxin B sulfate.
11-Digit NDC Billing Format:
67296066101
NDC to RxNorm Crosswalk:
  • RxCUI: 308511 - bacitracin zinc 500 UNT / polymyxin B sulfate 10,000 UNT per GM Ophthalmic Ointment
  • RxCUI: 308511 - bacitracin 0.5 UNT/MG / polymyxin B 10 UNT/MG Ophthalmic Ointment
  • RxCUI: 308511 - bacitracin (as bacitracin zinc) 500 UNT / polymyxin B (as polymyxin B sulfate) 10,000 UNT per GM Ophthalmic Ointment
Product Type:
Human Prescription Drug
Labeler Name:
Redpharm Drug
Dosage Form:
Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s):
Ophthalmic - Administration to the external eye.
Sample Package:
No
FDA Application Number:
ANDA064046
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
04-25-2008
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.

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Frequently Asked Questions

What is NDC 67296-0661-1?

The NDC Packaged Code 67296-0661-1 is assigned to a package of 1 tube in 1 carton / 3.5 g in 1 tube of Bacitracin Zinc And Polymyxin B Sulfate, a human prescription drug labeled by Redpharm Drug. The product's dosage form is ointment and is administered via ophthalmic form.

Is NDC 67296-0661 included in the NDC Directory?

Yes, Bacitracin Zinc And Polymyxin B Sulfate with product code 67296-0661 is active and included in the NDC Directory. The product was first marketed by Redpharm Drug on April 25, 2008 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 67296-0661-1?

The 11-digit format is 67296066101. 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
5-4-167296-0661-15-4-267296-0661-01