Senna Leaf And Docusate Sodium
NDC Package 65437-035-70

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Senna Leaf And Docusate Sodium is take preferably at bedtime or as directed by a doctoragestarting dosagemaximum dosageadults and children 12 years of age or older2 tablets once a day4 tablets twice a daychildren 6 to under 12 years1 tablet once a day2 tablets twice a daychildren 2 to under 6 years1/2 tablet once a day1 tablet twice a daychildren under 2 yearsask a doctorask a doctor. Marketed by Himprit Pharmachem Pvt Ltd, this product is identified by NDC 65437-035 and is authorized under FDA application part334.

Identification & Billing

NDC Package Code
65437-035-70
Package Description
1 BAG in 1 DRUM / 75000 TABLET, FILM COATED in 1 BAG
Product Code
11-Digit Billing Format
65437003570
RxNorm Crosswalk
  • RxCUI: 998740 - sennosides 8.6 MG / docusate sodium 50 MG Oral Tablet
  • RxCUI: 998740 - docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet
  • RxCUI: 998740 - DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet

Clinical Specifications

Proprietary Name
Senna Leaf And Docusate Sodium
Dosage Form
-
Usage Information
Take preferably at bedtime or as directed by a doctoragestarting dosagemaximum dosageadults and children 12 years of age or older2 tablets once a day4 tablets twice a daychildren 6 to under 12 years1 tablet once a day2 tablets twice a daychildren 2 to under 6 years1/2 tablet once a day1 tablet twice a daychildren under 2 yearsask a doctorask a doctor

Regulatory & Marketing

Labeler Name
Himprit Pharmachem Pvt Ltd
FDA Application #
part334
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
04-01-2010
Listing Expiration
12-31-2018
Exclude Flag
I
Sample Package
No

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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (65437-035). Click a package code to view its specific billing and regulatory data.

1 BAG in 1 DRUM / 50000 TABLET, FILM COATED in 1 BAG

* 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 65437-035-70 identifies a specific commercial package of 1 bag in 1 drum / 75000 tablet, film coated in 1 bag of Senna Leaf And Docusate Sodium, labeled by Himprit Pharmachem Pvt Ltd. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Himprit Pharmachem Pvt Ltd on April 01, 2010. The current certification is valid through December 31, 2018.

How is this Himprit Pharmachem Pvt Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 65437003570. 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)
65437-035-70
11-Digit CMS (5-4-2)
65437-0035-70

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