NDC Package 50090-5275-0 Prednisolone Acetate

Suspension/ Drops Ophthalmic - View Billable Units, 11-Digit Format, RxNorm

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:
50090-5275-0
Package Description:
1 BOTTLE, DROPPER in 1 CARTON / 5 mL in 1 BOTTLE, DROPPER
Product Code:
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:
50090527500
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1376336 - prednisoLONE acetate 1 % Ophthalmic Suspension
  • RxCUI: 1376336 - prednisolone acetate 10 MG/ML Ophthalmic Suspension
  • RxCUI: 1376336 - prednisolone acetate 1 % Ophthalmic Suspension
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    A-s Medication Solutions
    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):
    Sample Package:
    No
    FDA Application Number:
    NDA017011
    Marketing Category:
    NDA AUTHORIZED GENERIC - A product marketed as a "generic" drug under an approved New Drug Application (NDA), rather than an Abbreviated New Drug Application (ANDA),.
    Start Marketing Date:
    08-19-1997
    Listing Expiration Date:
    12-31-2025
    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 50090-5275-0?

    The NDC Packaged Code 50090-5275-0 is assigned to a package of 1 bottle, dropper in 1 carton / 5 ml in 1 bottle, dropper of Prednisolone Acetate, a human prescription drug labeled by A-s Medication Solutions. The product's dosage form is suspension/ drops and is administered via ophthalmic form.

    Is NDC 50090-5275 included in the NDC Directory?

    Yes, Prednisolone Acetate with product code 50090-5275 is active and included in the NDC Directory. The product was first marketed by A-s Medication Solutions on August 19, 1997 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 50090-5275-0?

    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 50090-5275-0?

    The 11-digit format is 50090527500. 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
    5-4-150090-5275-05-4-250090-5275-00