Sanatos
NDC Package 14505-399-06

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

Sanatos is other information: Store at controlled room temperature 15-30 C (59-86F)each tablespoon contains: potassium 5 mg, sodium 18 mg. Marketed by Pharmalab Enterprises Inc, this product is identified by NDC 14505-399 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
14505-399-06
Package Description
177 mL in 1 BOTTLE, PLASTIC
Product Code
14505-399
11-Digit Billing Format
14505039906
RxNorm Crosswalk
  • RxCUI: 1042684 - acetaminophen 500 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG in 15 mL Oral Solution
  • RxCUI: 1042684 - acetaminophen 33.3 MG/ML / dextromethorphan hydrobromide 1 MG/ML / doxylamine succinate 0.417 MG/ML Oral Solution
  • RxCUI: 1042684 - acetaminophen 1000 MG / dextromethorphan hydrobromide 30 MG / doxylamine succinate 12.5 MG per 30 ML Oral Solution
  • RxCUI: 1042684 - acetaminophen 500 MG / dextromethorphan hydrobromide 15 MG / doxylamine succinate 6.25 MG per 15 ML Oral Solution
  • RxCUI: 1042684 - APAP 33.3 MG/ML / Dextromethorphan Hydrobromide 1 MG/ML / doxylamine succinate 0.417 MG/ML Oral Solution

Clinical Specifications

Proprietary Name
Sanatos Night
Dosage Form
-
Usage Information
Other information: Store at controlled room temperature 15-30 C (59-86F)each tablespoon contains: potassium 5 mg, sodium 18 mg. Contains 10% alcohol.

Regulatory & Marketing

Labeler Name
Pharmalab Enterprises Inc
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
02-04-2010
Listing Expiration
12-31-2017
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 14505-399-06 identifies a specific commercial package of 177 ml in 1 bottle, plastic of Sanatos Night, labeled by Pharmalab Enterprises Inc. 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 Pharmalab Enterprises Inc on February 04, 2010. The current certification is valid through December 31, 2017.

How is this Pharmalab Enterprises Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 14505039906. 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)
14505-399-06
11-Digit CMS (5-4-2)
14505-0399-06

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