Ic Clear Lubricant Eye Drops
NDC Package 61660-500-10

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.

Ic Clear Lubricant Eye Drops is a . Marketed by Oboi Laboratories Pvt Ltd, this product is identified by NDC 61660-500 and is authorized under FDA application part349.

Identification & Billing

NDC Package Code
61660-500-10
Package Description
2 VIAL in 1 CARTON / 5 mL in 1 VIAL
Product Code
61660-500
11-Digit Billing Format
61660050010

Clinical Specifications

Proprietary Name
Ic Clear Lubricant Eye Drops
Dosage Form
-

Regulatory & Marketing

Labeler Name
Oboi Laboratories Pvt Ltd
FDA Application #
part349
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
08-01-2017
End Marketing Date
04-30-2020
Listing Expiration
04-30-2020
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 61660-500-10 identifies a specific commercial package of 2 vial in 1 carton / 5 ml in 1 vial of Ic Clear Lubricant Eye Drops, labeled by Oboi Laboratories Pvt Ltd. 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 Oboi Laboratories Pvt Ltd on August 01, 2017. The current certification is valid through April 30, 2020.

How is this Oboi Laboratories Pvt Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 61660050010. 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)
61660-500-10
11-Digit CMS (5-4-2)
61660-0500-10

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