NDC Package 24208-317-10 Sulfacetamide Sodium And Prednisolone Sodium Phosphate

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

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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:

24208-317-10

Package Description:

1 BOTTLE, DROPPER in 1 CARTON / 10 mL in 1 BOTTLE, DROPPER

Product Code:

24208-317

Proprietary Name:

Sulfacetamide Sodium And Prednisolone Sodium Phosphate

Non-Proprietary Name:

Sulfacetamide Sodium And Prednisolone Sodium Phosphate

Substance Name:

Prednisolone Sodium Phosphate; Sulfacetamide Sodium

Usage Information:

Sulfacetamide Sodium and Prednisolone Sodium Phosphate Ophthalmic Solution is indicated for corticosteroid-responsive inflammatory ocular conditions for which a corticosteroid is indicated and where superficial bacterial ocular infection or a risk of bacterial ocular infection exists.Ocular corticosteroids are indicated in inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe where the inherent risk of corticosteroid use in certain infective conjunctivitides is accepted to obtain diminution in edema and inflammation. They are also indicated in chronic anterior uveitis and corneal injury from chemical, radiation, or thermal burns or penetration of foreign bodies.The use of a combination drug with an anti-infective component is indicated where the risk of superficial ocular infection is high or where there is an expectation that potentially dangerous numbers of bacteria will be present in the eye.The particular anti-infective drug in this product is active against the following common bacterial eye pathogens: Escherichia coli, Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus (viridans group), Haemophilus influenzae, Klebsiella species, and Enterobacter species.This product does not provide adequate coverage against: Neisseria species, Serratia marcescens.A significant percentage of staphylococcal isolates are completely resistant to sulfa drugs.

11-Digit NDC Billing Format:

24208031710

Billing Unit:

ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

NDC to RxNorm Crosswalk:

RxCUI: 1012021 - prednisoLONE sodium phosphate 0.25 % / sulfacetamide sodium 10 % Ophthalmic Solution

RxCUI: 1012021 - prednisolone sodium phosphate 2.5 MG/ML / sulfacetamide sodium 100 MG/ML Ophthalmic Solution

RxCUI: 1012021 - prednisolone sodium phosphate 0.25 % / sulfacetamide sodium 10 % Ophthalmic Solution

Product Type:

Human Prescription Drug

Labeler Name:

Bausch & Lomb Incoporated

Dosage Form:

Solution/ Drops - A solution which is usually administered in a drop-wise fashion.

Administration Route(s):

Ophthalmic - Administration to the external eye.

Active Ingredient(s):

PREDNISOLONE SODIUM PHOSPHATE 2.3 mg/mL

SULFACETAMIDE SODIUM 100 mg/mL

Pharmacologic Class(es):

Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)

Corticosteroid - [EPC] (Established Pharmacologic Class)

Sulfonamide Antibacterial - [EPC] (Established Pharmacologic Class)

Sulfonamides - [CS]

Sample Package:

FDA Application Number:

ANDA074449

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

12-29-1995

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

24208 - Bausch & Lomb Incoporated
- 24208-317 - Sulfacetamide Sodium And Prednisolone Sodium Phosphate
  - 24208-317-10 - 1 BOTTLE, DROPPER in 1 CARTON / 10 mL in 1 BOTTLE, DROPPER

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 Code	Package Description
24208-317-05	1 BOTTLE, DROPPER in 1 CARTON / 5 mL in 1 BOTTLE, DROPPER

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 24208-317-10?

The NDC Packaged Code 24208-317-10 is assigned to a package of 1 bottle, dropper in 1 carton / 10 ml in 1 bottle, dropper of Sulfacetamide Sodium And Prednisolone Sodium Phosphate, a human prescription drug labeled by Bausch & Lomb Incoporated. The product's dosage form is solution/ drops and is administered via ophthalmic form.

Is NDC 24208-317 included in the NDC Directory?

Yes, Sulfacetamide Sodium And Prednisolone Sodium Phosphate with product code 24208-317 is active and included in the NDC Directory. The product was first marketed by Bausch & Lomb Incoporated on December 29, 1995 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 NDC billing unit for package 24208-317-10?

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 24208-317-10?

The 11-digit format is 24208031710. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	24208-317-10	5-4-2	24208-0317-10

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