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  5. NDC Package Code: 44118-807-30 Duet Dha 400

NDC Package 44118-807-30 Duet Dha 400

.beta.-carotene,Ascorbic Acid,Cholecalciferol,.alpha.-tocopherol Acetate,D-,Thiamine - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
44118-807-30
Package Description:
1 KIT in 1 CARTON * 30 TABLET in 1 BOTTLE (44118-803-30) * 30 CAPSULE, GELATIN COATED in 1 BOTTLE (44118-805-30)
Product Code:
44118-807
Proprietary Name:
Duet Dha 400
Non-Proprietary Name:
.beta.-carotene, Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol Acetate, D-, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Calcium Carbonate, Iron, Magnesium Oxide, Zinc Oxide, Cupric Oxide, Iodine, Omega-3 Fatty Acids
Usage Information:
This product is a gluten free prescription regimen of prenatal multi-vitamin, multi-mineral and omega-3 fatty acid supplements indicated for use in improving the nutritional status of women throughout pregnancy and in the post-natal period for both lactating and non-lactating mothers. This product is also useful in improving the nutritional status prior to conception.
11-Digit NDC Billing Format:
44118080730
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Product Type:
Human Prescription Drug
Labeler Name:
Eckson Labs, Llc
Dosage Form:
Kit - A packaged collection of related material.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    09-09-2011
    End Marketing Date:
    04-30-2024
    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 44118-807-30?

    The NDC Packaged Code 44118-807-30 is assigned to a package of 1 kit in 1 carton * 30 tablet in 1 bottle (44118-803-30) * 30 capsule, gelatin coated in 1 bottle (44118-805-30) of Duet Dha 400, a human prescription drug labeled by Eckson Labs, Llc. The product's dosage form is kit and is administered via oral form.

    Is NDC 44118-807 included in the NDC Directory?

    Yes, Duet Dha 400 with product code 44118-807 is active and included in the NDC Directory. The product was first marketed by Eckson Labs, Llc on September 09, 2011.

    What is the NDC billing unit for package 44118-807-30?

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

    What is the 11-digit format for NDC 44118-807-30?

    The 11-digit format is 44118080730. 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
    5-3-244118-807-305-4-244118-0807-30