NDC Package 66220-287-08 Caldolor

Ibuprofen Injection Intravenous - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
66220-287-08
Package Description:
25 VIAL in 1 CARTON / 8 mL in 1 VIAL
Product Code:
Proprietary Name:
Caldolor
Non-Proprietary Name:
Ibuprofen
Substance Name:
Ibuprofen
Usage Information:
Ibuprofen is used to help relieve mild to moderate pain. When used with an opioid (such as morphine), it may be used to relieve moderate to severe pain. It is also used to reduce fever. Ibuprofen is known as a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking your body's production of certain natural substances that cause inflammation. This effect helps to decrease swelling, pain, or fever.
11-Digit NDC Billing Format:
66220028708
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 2178273 - ibuprofen 800 MG in 200 ML Injection
  • RxCUI: 2178273 - 200 ML ibuprofen 4 MG/ML Injection
  • RxCUI: 2178273 - ibuprofen 800 MG per 200 ML Injection
  • RxCUI: 2178275 - Caldolor 800 MG in 200 ML Injection
  • RxCUI: 2178275 - 200 ML ibuprofen 4 MG/ML Injection [Caldolor]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Cumberland Pharmaceuticals Inc.
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA022348
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    06-11-2009
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 66220-287-08?

    The NDC Packaged Code 66220-287-08 is assigned to a package of 25 vial in 1 carton / 8 ml in 1 vial of Caldolor, a human prescription drug labeled by Cumberland Pharmaceuticals Inc.. The product's dosage form is injection and is administered via intravenous form.

    Is NDC 66220-287 included in the NDC Directory?

    Yes, Caldolor with product code 66220-287 is active and included in the NDC Directory. The product was first marketed by Cumberland Pharmaceuticals Inc. on June 11, 2009 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 66220-287-08?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 66220-287-08?

    The 11-digit format is 66220028708. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-266220-287-085-4-266220-0287-08