Docusate Sodium 50 Mg And Sennosides 8.6 Mg Capsule, Liquid Filled
NDC Package 72090-048-01

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 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.

Docusate Sodium 50 Mg And Sennosides 8.6 Mg capsules is a drug for further processing. This formulation utilizes a capsule, liquid filled delivery system. Marketed by Pioneer Life Sciences, Llc, this product is identified by NDC 72090-048.

Identification & Billing

NDC Package Code
72090-048-01
Package Description
18000 CAPSULE, LIQUID FILLED in 1 BOX
Product Code
72090-048
11-Digit Billing Format
72090004801

Clinical Specifications

Proprietary Name
Docusate Sodium 50 Mg And Sennosides 8.6 Mg
Non-Proprietary Name
Docusate Sodium 50 Mg And Sennosides 8.6 Mg
Substance Name
Docusate Sodium; Sennosides
Dosage Form
Capsule, Liquid Filled - A solid dosage form in which the drug is enclosed within a soluble, gelatin shell which is plasticized by the addition of a polyol, such as sorbitol or glycerin, and is therefore of a somewhat thicker consistency than that of a hard shell capsule; typically, the active ingredients are dissolved or suspended in a liquid vehicle.
Active Ingredient(s)

Regulatory & Marketing

Labeler Name
Pioneer Life Sciences, Llc
Product Type
Drug For Further Processing
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
04-30-2025
Listing Expiration
12-31-2026
Exclude Flag
N
Unfinished Product
Yes
Sample Package
N/A

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 72090-048-01 identifies a specific commercial package of 18000 capsule, liquid filled in 1 box of Docusate Sodium 50 Mg And Sennosides 8.6 Mg (UNFINISHED drug), drug for further processing labeled by Pioneer Life Sciences, Llc. This capsule, liquid filled is formulated for use and contains docusate sodium; sennosides as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Pioneer Life Sciences, Llc on April 30, 2025. The current certification is valid through December 31, 2026.

How is this Pioneer Life Sciences, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72090004801. 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)
72090-048-01
11-Digit CMS (5-4-2)
72090-0048-01

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