Prednisolone Sodium Phosphate
NDC Package 0574-0148-04

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Prednisolone Sodium Phosphate is prednisolone is a man-made form of a natural substance (corticosteroid hormone) made by the adrenal gland. Marketed by Paddock Laboratories, Llc, this product is identified by NDC 0574-0148 and is authorized under FDA application ANDA075988.

Identification & Billing

NDC Package Code
0574-0148-04
Package Description
120 mL in 1 BOTTLE
Product Code
0574-0148
11-Digit Billing Format
00574014804

Clinical Specifications

Proprietary Name
Prednisolone Sodium Phosphate
Dosage Form
-
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.

Regulatory & Marketing

Labeler Name
Paddock Laboratories, Llc
FDA Application #
ANDA075988
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
05-25-2004
End Marketing Date
05-31-2007
Listing Expiration
05-31-2007
Exclude Flag
D
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 0574-0148-04 identifies a specific commercial package of 120 ml in 1 bottle of Prednisolone Sodium Phosphate, labeled by Paddock Laboratories, Llc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Paddock Laboratories, Llc on May 25, 2004. The current certification is valid through May 31, 2007.

What are the primary indications for this medication?

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.

How is this Paddock Laboratories, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00574014804. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (4-4-2)
0574-0148-04
11-Digit CMS (5-4-2)
00574-0148-04

Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.