NDC Package 69238-2434-5 Ciprofloxacin

Tablet, Film Coated Oral - 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:
69238-2434-5
Package Description:
50 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Ciprofloxacin
Non-Proprietary Name:
Ciprofloxacin
Substance Name:
Ciprofloxacin Hydrochloride
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:
69238243405
NDC to RxNorm Crosswalk:
  • RxCUI: 197511 - ciprofloxacin 250 MG Oral Tablet
  • RxCUI: 197511 - ciprofloxacin 250 MG (as ciprofloxacin HCl 297 MG) Oral Tablet
  • RxCUI: 197512 - ciprofloxacin 750 MG Oral Tablet
  • RxCUI: 197512 - ciprofloxacin (as ciprofloxacin hydrochloride) 750 MG Oral Tablet
  • RxCUI: 199370 - ciprofloxacin 100 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Amneal Pharmaceuticals Ny Llc
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA075939
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-29-2024
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    69238-2434-1100 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 69238-2434-5?

    The NDC Packaged Code 69238-2434-5 is assigned to a package of 50 tablet, film coated in 1 bottle of Ciprofloxacin, a human prescription drug labeled by Amneal Pharmaceuticals Ny Llc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 69238-2434 included in the NDC Directory?

    Yes, Ciprofloxacin with product code 69238-2434 is active and included in the NDC Directory. The product was first marketed by Amneal Pharmaceuticals Ny Llc on February 29, 2024 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 69238-2434-5?

    The 11-digit format is 69238243405. 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
    5-4-169238-2434-55-4-269238-2434-05