NDC Package 0395-2775-16 Iodine And Potassium Iodide

Liquid - View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
0395-2775-16
Package Description:
473 mL in 1 BOTTLE, PLASTIC
Product Code:
Non-Proprietary Name:
Iodine And Potassium Iodide
Substance Name:
Iodine; Potassium Iodide
Usage Information:
Iodine should not be given to cases of active Tuberculosis, or those known to be sensitive to iodine, and discontinued in cases later developing a sensitivity to the iodine therapy.
11-Digit NDC Billing Format:
00395277516
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
473 ML
Product Type:
Human Prescription Drug
Labeler Name:
Humco Holding Group, Inc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Sample Package:
N/A
Marketing Category:
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date:
01-01-2008
Listing Expiration Date:
12-31-2024
Exclude Flag:
N
Unfinished Product:
Yes
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 0395-2775-16?

The NDC Packaged Code 0395-2775-16 is assigned to an UNFINISHED drug package of 473 ml in 1 bottle, plastic of Iodine And Potassium Iodide, a human prescription drug labeled by Humco Holding Group, Inc.. The product's dosage form is liquid and is administered via form.This product is billed per "ML" milliliter and contains an estimated amount of 473 billable units per package.

Is NDC 0395-2775 included in the NDC Directory?

Yes, Iodine And Potassium Iodide is an UNFINISHED PRODUCT with code 0395-2775 that is active and included in the NDC Directory. The product was first marketed by Humco Holding Group, Inc. on January 01, 2008 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 0395-2775-16?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 473.

What is the 11-digit format for NDC 0395-2775-16?

The 11-digit format is 00395277516. 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 4-4-2 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
4-4-20395-2775-165-4-200395-2775-16