1. Home
  2. Labeler Index
  3. Bausch & Lomb Incorporated
  4. 24208-715
  5. NDC Package Code: 24208-715-10 Prednisolone Sodium Phosphate

NDC Package 24208-715-10 Prednisolone Sodium Phosphate

Solution/ Drops Ophthalmic - 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:
24208-715-10
Package Description:
1 BOTTLE, DROPPER in 1 CARTON / 10 mL in 1 BOTTLE, DROPPER
Product Code:
24208-715
Proprietary Name:
Prednisolone Sodium Phosphate
Non-Proprietary Name:
Prednisolone Sodium Phosphate
Substance Name:
Prednisolone Sodium Phosphate
Usage Information:
Prednisolone is a man-made form of a natural substance (corticosteroid hormone) made by the adrenal gland. It is used to treat conditions such as arthritis, blood problems, immune system disorders, skin and eye conditions, breathing problems, cancer, and severe allergies. It decreases your immune system's response to various diseases to reduce symptoms such as pain, swelling and allergic-type reactions.
11-Digit NDC Billing Format:
24208071510
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 314165 - prednisoLONE sodium phosphate 1 % Ophthalmic Solution
  • RxCUI: 314165 - prednisolone 10 MG/ML Ophthalmic Solution
  • RxCUI: 314165 - prednisolone sodium phosphate 1 % Ophthalmic Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Bausch & Lomb Incorporated
    Dosage Form:
    Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
    • Active Ingredient(s):
  • PREDNISOLONE SODIUM PHOSPHATE 10 mg/mL
    • Pharmacologic Class(es):
  • Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)
  • Corticosteroid - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA040070
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-29-1994
    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 24208-715-10?

    The NDC Packaged Code 24208-715-10 is assigned to a package of 1 bottle, dropper in 1 carton / 10 ml in 1 bottle, dropper of Prednisolone Sodium Phosphate, a human prescription drug labeled by Bausch & Lomb Incorporated. The product's dosage form is solution/ drops and is administered via ophthalmic form.

    Is NDC 24208-715 included in the NDC Directory?

    Yes, Prednisolone Sodium Phosphate with product code 24208-715 is active and included in the NDC Directory. The product was first marketed by Bausch & Lomb Incorporated on July 29, 1994 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 NDC billing unit for package 24208-715-10?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 24208-715-10?

    The 11-digit format is 24208071510. 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
    5-3-224208-715-105-4-224208-0715-10