Vaprisol Dextrose In Plastic Container
NDC Package 66220-160-10

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.

Vaprisol Dextrose In Plastic Container is a . Marketed by Cumberland Pharmaceuticals Inc., this product is identified by NDC 66220-160 and is authorized under FDA application NDA021697.

Identification & Billing

NDC Package Code
66220-160-10
Package Description
1 BAG in 1 BOX / 1 POUCH in 1 BAG / 100 mL in 1 POUCH
Product Code
66220-160
11-Digit Billing Format
66220016010
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

Clinical Specifications

Proprietary Name
Vaprisol Dextrose In Plastic Container
Dosage Form
-

Regulatory & Marketing

Labeler Name
Cumberland Pharmaceuticals Inc.
FDA Application #
NDA021697
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
10-08-2008
End Marketing Date
12-31-2023
Listing Expiration
12-31-2023
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 66220-160-10 identifies a specific commercial package of 1 bag in 1 box / 1 pouch in 1 bag / 100 ml in 1 pouch of Vaprisol Dextrose In Plastic Container, labeled by Cumberland 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 Cumberland Pharmaceuticals Inc. on October 08, 2008. The current certification is valid through December 31, 2023.

How is this Cumberland Pharmaceuticals Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 66220016010. 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)
66220-160-10
11-Digit CMS (5-4-2)
66220-0160-10

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