NDC Package 17856-1304-2 Docusate Sodium Liquid

View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

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:

17856-1304-2

Package Description:

72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 10 mL in 1 CUP, UNIT-DOSE

Product Code:

17856-1304

Proprietary Name:

Docusate Sodium Liquid

Usage Information:

UsesRelief of occasional constipation

11-Digit NDC Billing Format:

17856130402

NDC to RxNorm Crosswalk:

RxCUI: 1248119 - docusate sodium 50 MG in 5 mL Oral Suspension
RxCUI: 1248119 - docusate sodium 10 MG/ML Oral Suspension
RxCUI: 1248119 - docusate sodium 100 MG per 10 ML Oral Suspension
RxCUI: 1248119 - docusate sodium 150 MG per 15 ML Oral Suspension
RxCUI: 1248119 - docusate sodium 50 MG per 5 ML Oral Suspension

Labeler Name:

Atlantic Biologicals Corp.

Sample Package:

FDA Application Number:

M007

Marketing Category:

OTC MONOGRAPH DRUG -

Start Marketing Date:

10-01-2020

Listing Expiration Date:

12-31-2026

Exclude Flag:

Code Structure:

17856 - Atlantic Biologicals Corp.
- 17856-1304 - Docusate Sodium Liquid
  - 17856-1304-2 - 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 10 mL in 1 CUP, UNIT-DOSE

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.

Other Product Packages

The following packages are also available for this product:

NDC Package Code	Package Description
17856-1304-1	50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 25 mL in 1 CUP, UNIT-DOSE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 17856-1304-2?

The NDC Packaged Code 17856-1304-2 is assigned to a package of 72 cup, unit-dose in 1 box, unit-dose / 10 ml in 1 cup, unit-dose of Docusate Sodium Liquid, labeled by Atlantic Biologicals Corp.. The product's dosage form is and is administered via form.

Is NDC 17856-1304 included in the NDC Directory?

No, Docusate Sodium Liquid with product code 17856-1304 is excluded from the NDC Directory for failure to respond to FDA's requests for correction to deficient or non-compliant submissions. The product was first marketed by Atlantic Biologicals Corp. on October 01, 2020 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 17856-1304-2?

The 11-digit format is 17856130402. 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 5-4-1 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
5-4-1	17856-1304-2	5-4-2	17856-1304-02

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