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  5. NDC Package Code: 17856-0759-3 Prednisolone Sodium Phosphate

NDC Package 17856-0759-3 Prednisolone Sodium Phosphate

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
17856-0759-3
Package Description:
48 SYRINGE in 1 BOX, UNIT-DOSE / 5 mL in 1 SYRINGE
Product Code:
17856-0759
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:
17856075903
NDC to RxNorm Crosswalk:
  • RxCUI: 283077 - prednisoLONE sodium phosphate 15 MG in 5 mL Oral Solution
  • RxCUI: 283077 - prednisolone 3 MG/ML Oral Solution
  • RxCUI: 283077 - prednisolone 15 MG (as prednisolone sodium phosphate 20.2 MG) per 5 ML Oral Solution
  • RxCUI: 283077 - prednisolone 15 MG per 5 ML Oral Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Atlantic Biologicals Corp.
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • PREDNISOLONE SODIUM PHOSPHATE 15 mg/5mL
    • Pharmacologic Class(es):
  • Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)
  • Corticosteroid - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA076913
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-25-2005
    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
    17856-0759-15 mL in 1 SYRINGE, PLASTIC
    17856-0759-61 BOX in 1 CUP, UNIT-DOSE / 72 CUP, UNIT-DOSE in 1 BOX (17856-0759-2) / 10 mL in 1 CUP, UNIT-DOSE
    17856-0759-71 BOX, UNIT-DOSE in 1 CUP, UNIT-DOSE / 72 CUP in 1 BOX, UNIT-DOSE / 5 mL in 1 CUP (17856-0759-5)
    17856-0759-81 BOX, UNIT-DOSE in 1 SYRINGE / 48 SYRINGE in 1 BOX, UNIT-DOSE / 2.5 mL in 1 SYRINGE (17856-0759-4)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 17856-0759-3?

    The NDC Packaged Code 17856-0759-3 is assigned to a package of 48 syringe in 1 box, unit-dose / 5 ml in 1 syringe of Prednisolone Sodium Phosphate, a human prescription drug labeled by Atlantic Biologicals Corp.. The product's dosage form is solution and is administered via oral form.

    Is NDC 17856-0759 included in the NDC Directory?

    Yes, Prednisolone Sodium Phosphate with product code 17856-0759 is active and included in the NDC Directory. The product was first marketed by Atlantic Biologicals Corp. on April 25, 2005 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 17856-0759-3?

    The 11-digit format is 17856075903. 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
    5-4-117856-0759-35-4-217856-0759-03