1. Home
  2. Labeler Index
  3. Sato Pharmaceutical Co., Ltd.
  4. 49873-404
  5. NDC Package Code: 49873-404-01 Sankaijo

NDC Package 49873-404-01 Sankaijo

Docusate Sodium,Sennosides Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
49873-404-01
Package Description:
1 BOTTLE in 1 CARTON / 150 TABLET in 1 BOTTLE
Product Code:
49873-404
Proprietary Name:
Sankaijo
Non-Proprietary Name:
Docusate Sodium, Sennosides
Substance Name:
Docusate Sodium; Sennosides
Usage Information:
Uses■for the relief of occasional constipation (irregularity) ■generally produces bowel movement in 6 to 12 hours
11-Digit NDC Billing Format:
49873040401
NDC to RxNorm Crosswalk:
  • RxCUI: 1235252 - docusate sodium 8.33 MG / sennosides 1.36 MG Oral Tablet
  • RxCUI: 1235252 - docusate sodium 8.33 MG / sennosides, USP 1.36 MG Oral Tablet
  • RxCUI: 1235252 - DOSS Sodium 8.33 MG / sennosides, USP 1.36 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Sato Pharmaceutical Co., Ltd.
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • DOCUSATE SODIUM 8.33 mg/1
  • SENNOSIDES 1.36 mg/1
    • Sample Package:
    No
    FDA Application Number:
    M007
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    12-20-2002
    Listing Expiration Date:
    12-31-2024
    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.

    Frequently Asked Questions

    What is NDC 49873-404-01?

    The NDC Packaged Code 49873-404-01 is assigned to a package of 1 bottle in 1 carton / 150 tablet in 1 bottle of Sankaijo, a human over the counter drug labeled by Sato Pharmaceutical Co., Ltd.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 49873-404 included in the NDC Directory?

    Yes, Sankaijo with product code 49873-404 is active and included in the NDC Directory. The product was first marketed by Sato Pharmaceutical Co., Ltd. on December 20, 2002 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 49873-404-01?

    The 11-digit format is 49873040401. 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 5-3-2 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
    5-3-249873-404-015-4-249873-0404-01