NDC Package 0615-8331-28 Senexon-s

Docusate Sodium 50mg And Sennosides 8.6mg Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

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:
0615-8331-28
Package Description:
28 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Senexon-s
Non-Proprietary Name:
Docusate Sodium 50mg And Sennosides 8.6mg
Substance Name:
Docusate Sodium; Sennosides
Usage Information:
Take preferably at bedtime or as directed by a doctoragestarting dosagemaximum dosageadults and children 12 years and over2 tablets once a day  4 tablets twice a daychildren 6 to under 12 years1 tablet once a day 2 tablets twice a daychildren 2 to under 6 years 1/2 tablet once a day 1 tablet twice a daychildren under 2 yearsask a doctor ask a doctor
11-Digit NDC Billing Format:
00615833128
NDC to RxNorm Crosswalk:
  • RxCUI: 1248013 - Senexon-S 50 MG / 8.6 MG Oral Tablet
  • RxCUI: 1248013 - docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet [Senexon S]
  • RxCUI: 1248013 - DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet [Senexon S]
  • RxCUI: 1248013 - Senexon-S (docusate sodium 50 MG / sennosides, USP 8.6 MG) Oral Tablet
  • RxCUI: 998740 - sennosides 8.6 MG / docusate sodium 50 MG Oral Tablet
Product Type:
Human Otc Drug
Labeler Name:
Ncs Healthcare Of Ky, Llc Dba Vangard Labs
Dosage Form:
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Sample Package:
No
FDA Application Number:
505G(a)(3)
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
10-02-2019
Listing Expiration Date:
12-31-2026
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
0615-8331-0515 TABLET, FILM COATED in 1 BLISTER PACK
0615-8331-3930 TABLET, FILM COATED in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0615-8331-28?

The NDC Packaged Code 0615-8331-28 is assigned to a package of 28 tablet, film coated in 1 blister pack of Senexon-s, a human over the counter drug labeled by Ncs Healthcare Of Ky, Llc Dba Vangard Labs. The product's dosage form is tablet, film coated and is administered via oral form.

Is NDC 0615-8331 included in the NDC Directory?

Yes, Senexon-s with product code 0615-8331 is active and included in the NDC Directory. The product was first marketed by Ncs Healthcare Of Ky, Llc Dba Vangard Labs on October 02, 2019 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 0615-8331-28?

The 11-digit format is 00615833128. 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
4-4-20615-8331-285-4-200615-8331-28