NDC Package 57664-224-88 Oxycodone Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Package Information
Frequently Asked Questions

Package Information

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

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:

57664-224-88

Package Description:

100 TABLET in 1 BOTTLE

Product Code:

57664-224

Proprietary Name:

Oxycodone Hydrochloride

Usage Information:

Oxycodone hydrochloride tablets are indicated for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate.Limitations of UseBecause of the risks of addiction, abuse, and misuse with opioids, even at recommended doses [see Warnings and Precautions (5.1)], reserve oxycodone hydrochloride tablets for use in patients for whom alternative treatment options (e.g., non-opioid analgesics or opioid combination products):•Have not been tolerated or are not expected to be tolerated,Have not provided adequate analgesia or are not expected to provide adequate analgesia.

11-Digit NDC Billing Format:

57664022488

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

100 EA

Labeler Name:

Sun Pharmaceutical Industries, Inc.

Sample Package:

FDA Application Number:

ANDA090659

Marketing Category:

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

Start Marketing Date:

05-12-2009

End Marketing Date:

09-30-2021

Listing Expiration Date:

09-30-2021

Exclude Flag:

Code Structure:

57664 - Sun Pharmaceutical Industries, Inc.
- 57664-224 - Oxycodone Hydrochloride
  - 57664-224-88 - 100 TABLET in 1 BOTTLE

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.

Frequently Asked Questions

What is NDC 57664-224-88?

The NDC Packaged Code 57664-224-88 is assigned to a package of 100 tablet in 1 bottle of Oxycodone Hydrochloride, labeled by Sun Pharmaceutical Industries, Inc.. The product's dosage form is and is administered via form.

Is NDC 57664-224 included in the NDC Directory?

No, Oxycodone Hydrochloride with product code 57664-224 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Sun Pharmaceutical Industries, Inc. on May 12, 2009 and its listing in the NDC Directory is set to expire on September 30, 2021 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 57664-224-88?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 100.

What is the 11-digit format for NDC 57664-224-88?

The 11-digit format is 57664022488. 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	57664-224-88	5-4-2	57664-0224-88

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