NDC Package 60687-622-01 Sennosides And Docusate Sodium

Tablet 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:
60687-622-01
Package Description:
100 BLISTER PACK in 1 BOX, UNIT-DOSE / 1 TABLET in 1 BLISTER PACK (60687-622-11)
Product Code:
Proprietary Name:
Sennosides And Docusate Sodium
Non-Proprietary Name:
Sennosides And Docusate Sodium
Substance Name:
Docusate Sodium; Sennosides
Usage Information:
Do not exceed 8 tablets in 24 hours Adults and children 12 years of age and older take 2 tablets once a day preferably at bedtime; increase as needed, or as directed by a doctor; the maximum dose should be 4 tablets in the morning and 4 tablets at bedtime Children under 12 years ask a doctor
11-Digit NDC Billing Format:
60687062201
NDC to 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
  • Product Type:
    Human Otc Drug
    Labeler Name:
    American Health Packaging
    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.
  • Sample Package:
    No
    FDA Application Number:
    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:
    08-03-2021
    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 60687-622-01?

    The NDC Packaged Code 60687-622-01 is assigned to a package of 100 blister pack in 1 box, unit-dose / 1 tablet in 1 blister pack (60687-622-11) of Sennosides And Docusate Sodium, a human over the counter drug labeled by American Health Packaging. The product's dosage form is tablet and is administered via oral form.

    Is NDC 60687-622 included in the NDC Directory?

    Yes, Sennosides And Docusate Sodium with product code 60687-622 is active and included in the NDC Directory. The product was first marketed by American Health Packaging on August 03, 2021 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 60687-622-01?

    The 11-digit format is 60687062201. 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
    5-3-260687-622-015-4-260687-0622-01