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  5. NDC Package Code: 85293-003-01 Ciprofloxacin

NDC Package 85293-003-01 Ciprofloxacin

Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
85293-003-01
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
85293-003
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:
85293000301
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Umasuto, Llc
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
CIPROFLOXACIN HYDROCHLORIDE 500 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA076639
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
03-05-2025
Listing Expiration Date:
12-31-2026
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 85293-003-01?

The NDC Packaged Code 85293-003-01 is assigned to a package of 100 tablet in 1 bottle of Ciprofloxacin, a human prescription drug labeled by Umasuto, Llc. The product's dosage form is tablet and is administered via oral form.

Is NDC 85293-003 included in the NDC Directory?

Yes, Ciprofloxacin with product code 85293-003 is active and included in the NDC Directory. The product was first marketed by Umasuto, Llc on March 05, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 85293-003-01?

The 11-digit format is 85293000301. 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 5-3-2 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
5-3-285293-003-015-4-285293-0003-01