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  5. NDC Package Code: 42799-815-01 Prednisolone Sodium Phosphate

NDC Package 42799-815-01 Prednisolone Sodium Phosphate

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

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    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:
42799-815-01
Package Description:
237 mL in 1 BOTTLE, PLASTIC
Product Code:
42799-815
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:
42799081501
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
237 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 249066 - prednisoLONE sodium phosphate 25 MG in 5 mL Oral Solution
  • RxCUI: 249066 - prednisolone 5 MG/ML Oral Solution
  • RxCUI: 249066 - prednisolone 25 MG (prednisolone sodium phosphate 33.6 MG) per 5 ML Oral Solution
  • RxCUI: 283077 - prednisoLONE sodium phosphate 15 MG in 5 mL Oral Solution
  • RxCUI: 283077 - prednisolone 3 MG/ML Oral Solution
Product Type:
Human Prescription Drug
Labeler Name:
Edenbridge Pharmaceuticals Llc.
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):
Sample Package:
No
FDA Application Number:
ANDA203559
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
10-09-2023
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.

NDC HCPCS Crosswalk

This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

NDC 42799-815-01 HCPCS crosswalk information with package details and bill units information.

NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
42799081501J7510PREDNISOLONE ORAL, PER 5 MG5 MG237ML

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 42799-815-01?

The NDC Packaged Code 42799-815-01 is assigned to a package of 237 ml in 1 bottle, plastic of Prednisolone Sodium Phosphate, a human prescription drug labeled by Edenbridge Pharmaceuticals Llc.. The product's dosage form is solution and is administered via oral form.

Is NDC 42799-815 included in the NDC Directory?

Yes, Prednisolone Sodium Phosphate with product code 42799-815 is active and included in the NDC Directory. The product was first marketed by Edenbridge Pharmaceuticals Llc. on October 09, 2023 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 NDC billing unit for package 42799-815-01?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 237.

What is the 11-digit format for NDC 42799-815-01?

The 11-digit format is 42799081501. 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
5-3-242799-815-015-4-242799-0815-01