Phospholine Iodide
NDC Package 53270-102-65

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

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

Phospholine Iodide is a medication used to treat high pressure inside the eye (due to conditions such as certain types of glaucoma) and other eye problems (such as accommodative esotropia). Marketed by Cangene Biopharma Inc, this product is identified by NDC 53270-102 and is authorized under FDA application NDA011963.

Identification & Billing

NDC Package Code
53270-102-65
Package Description
5 mL in 1 PACKAGE
Product Code
11-Digit Billing Format
53270010265

Clinical Specifications

Proprietary Name
Phospholine Iodide
Dosage Form
-
Usage Information
This medication is used to treat high pressure inside the eye (due to conditions such as certain types of glaucoma) and other eye problems (such as accommodative esotropia). It works by causing the pupil to shrink, decreasing the amount of fluid within the eye, and affecting certain eye muscles.

Regulatory & Marketing

Labeler Name
Cangene Biopharma Inc
FDA Application #
NDA011963
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
12-01-2005
End Marketing Date
02-25-2010
Listing Expiration
02-25-2010
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 53270-102-65 identifies a specific commercial package of 5 ml in 1 package of Phospholine Iodide, labeled by Cangene Biopharma Inc. 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 Cangene Biopharma Inc on December 01, 2005. The current certification is valid through February 25, 2010.

What are the primary indications for this medication?

This medication is used to treat high pressure inside the eye (due to conditions such as certain types of glaucoma) and other eye problems (such as accommodative esotropia). It works by causing the pupil to shrink, decreasing the amount of fluid within the eye, and affecting certain eye muscles.

How is this Cangene Biopharma Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 53270010265. 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 (5-3-2)
53270-102-65
11-Digit CMS (5-4-2)
53270-0102-65

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