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  5. NDC Package Code: 60219-2550-1 Prednisolone Acetate

NDC Package 60219-2550-1 Prednisolone Acetate

Suspension/ 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:
60219-2550-1
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 5 mL in 1 BOTTLE, PLASTIC
Product Code:
60219-2550
Proprietary Name:
Prednisolone Acetate
Non-Proprietary Name:
Prednisolone Acetate
Substance Name:
Prednisolone Acetate
Usage Information:
This medication is used to treat certain eye conditions due to inflammation or injury. Prednisolone works by relieving symptoms such as swelling, redness, and itching. It belongs to a class of drugs known as corticosteroids.
11-Digit NDC Billing Format:
60219255001
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Amneal Pharmaceuticals Ny Llc
Dosage Form:
Suspension/ Drops - A suspension which is usually administered in a dropwise fashion.
Administration Route(s):
Ophthalmic - Administration to the external eye.
Active Ingredient(s):
PREDNISOLONE ACETATE 10 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA218256
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
06-13-2025
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 60219-2550-1?

The NDC Packaged Code 60219-2550-1 is assigned to a package of 1 bottle, plastic in 1 carton / 5 ml in 1 bottle, plastic of Prednisolone Acetate, a human prescription drug labeled by Amneal Pharmaceuticals Ny Llc. The product's dosage form is suspension/ drops and is administered via ophthalmic form.

Is NDC 60219-2550 included in the NDC Directory?

Yes, Prednisolone Acetate with product code 60219-2550 is active and included in the NDC Directory. The product was first marketed by Amneal Pharmaceuticals Ny Llc on June 13, 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 60219-2550-1?

The 11-digit format is 60219255001. 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
5-4-160219-2550-15-4-260219-2550-01