NDC Package 53002-9271-1 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:
53002-9271-1
Package Description:
3.5 g in 1 BOTTLE, DROPPER
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:
This product is contraindicated in those individuals who have shown hypersensitivity to any of its components.
11-Digit NDC Billing Format:
53002927101
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:
    Rpk Pharmaceuticals, Inc.
    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:
    12-31-2024
    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 53002-9271-1?

    The NDC Packaged Code 53002-9271-1 is assigned to a package of 3.5 g in 1 bottle, dropper of Bacitracin Zinc And Polymyxin B Sulfate, a human prescription drug labeled by Rpk Pharmaceuticals, Inc.. The product's dosage form is ointment and is administered via ophthalmic form.

    Is NDC 53002-9271 included in the NDC Directory?

    Yes, Bacitracin Zinc And Polymyxin B Sulfate with product code 53002-9271 is active and included in the NDC Directory. The product was first marketed by Rpk Pharmaceuticals, Inc. on April 25, 2008 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 53002-9271-1?

    The 11-digit format is 53002927101. 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
    5-4-153002-9271-15-4-253002-9271-01