Oxycodone Hydrochloride
NDC Package 68462-347-37

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.

Oxycodone Hydrochloride is a . Marketed by Glenmark Pharmaceuticals, Inc, this product is identified by NDC 68462-347 and is authorized under FDA application NDA200535.

Identification & Billing

NDC Package Code
68462-347-37
Package Description
1 BOTTLE, PLASTIC in 1 CARTON / 30 mL in 1 BOTTLE, PLASTIC
Product Code
68462-347
11-Digit Billing Format
68462034737
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

Clinical Specifications

Proprietary Name
Oxycodone Hydrochloride
Dosage Form
-

Regulatory & Marketing

Labeler Name
Glenmark Pharmaceuticals, Inc
FDA Application #
NDA200535
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
12-20-2010
End Marketing Date
11-14-2023
Listing Expiration
11-14-2023
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 68462-347-37 identifies a specific commercial package of 1 bottle, plastic in 1 carton / 30 ml in 1 bottle, plastic of Oxycodone Hydrochloride, labeled by Glenmark Pharmaceuticals, 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 Glenmark Pharmaceuticals, Inc on December 20, 2010. The current certification is valid through November 14, 2023.

How is this Glenmark Pharmaceuticals, Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68462034737. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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)
68462-347-37
11-Digit CMS (5-4-2)
68462-0347-37

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