Oxycodone Hydchloride Tablet
NDC Package 49999-899-00

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Oxycodone Hydchloride tablets is oxycodone hydrochloride tablets are an immediate-release oral formulation of oxycodone hydrochloride indicated for the management of moderate to severe pain where the use of an opioid analgesic is appropriate. This formulation utilizes a tablet delivery system. Marketed by Quality Care Products Llc, this product is identified by NDC 49999-899 and is authorized under FDA application ANDA091393.

Identification & Billing

NDC Package Code
49999-899-00
Package Description
100 TABLET in 1 BOTTLE
Product Code
49999-899
11-Digit Billing Format
49999089900
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Oxycodone Hydchloride
Non-Proprietary Name
Oxycodone Hydchloride
Substance Name
Oxycodone Hydrochloride
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
OXYCODONE HYDROCHLORIDE 5 mg/1
Pharmacologic Class
Usage Information
Oxycodone hydrochloride tablets are an immediate-release oral formulation of oxycodone hydrochloride indicated for the management of moderate to severe pain where the use of an opioid analgesic is appropriate.
DEA Schedule
Schedule II (CII) Substances

Regulatory & Marketing

Labeler Name
Quality Care Products Llc
Product Type
Human Prescription Drug
FDA Application #
ANDA091393
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
12-20-2011
End Marketing Date
06-30-2027
Exclude Flag
N
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (49999-899). Click a package code to view its specific billing and regulatory data.

49999-899-15
15 TABLET in 1 BOTTLE
49999-899-21
21 TABLET in 1 BOTTLE
49999-899-30
30 TABLET in 1 BOTTLE
49999-899-40
40 TABLET in 1 BOTTLE
49999-899-60
60 TABLET in 1 BOTTLE
49999-899-90
90 TABLET in 1 BOTTLE

* 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 49999-899-00 identifies a specific commercial package of 100 tablet in 1 bottle of Oxycodone Hydchloride, a human prescription drug labeled by Quality Care Products Llc. This tablet is formulated for oral use and contains oxycodone hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Quality Care Products Llc on December 20, 2011.

How is this Quality Care Products Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49999089900. 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)
49999-899-00
11-Digit CMS (5-4-2)
49999-0899-00

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