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  4. NDC Product Code: 71610-219 Bisacodyl

NDC 71610-219 Bisacodyl

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 71610-219?
  5. Bisacodyl Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71610-219
Proprietary Name:
Bisacodyl
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aphena Pharma Solutions - Tennessee, Llc
Labeler Code:
71610
Product Label ID:
b5e1a7f8-17ef-4d67-aeea-879603f800a5
Start Marketing Date: [9]
12-01-2018
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
Shape:
ROUND (C48348)
Size(s):
6 MM
Imprint(s):
5
Score:
1

Product Packages

NDC Code 71610-219-02

Package Description: 2 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Code 71610-219-03

Package Description: 3 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Code 71610-219-04

Package Description: 4 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Code 71610-219-08

Package Description: 8 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Code 71610-219-20

Package Description: 20 TABLET, COATED in 1 BOTTLE, PLASTIC

Product Details

What is NDC 71610-219?

The NDC code 71610-219 is assigned by the FDA to the product Bisacodyl which is product labeled by Aphena Pharma Solutions - Tennessee, Llc. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 71610-219-02 2 tablet, coated in 1 bottle, plastic , 71610-219-03 3 tablet, coated in 1 bottle, plastic , 71610-219-04 4 tablet, coated in 1 bottle, plastic , 71610-219-08 8 tablet, coated in 1 bottle, plastic , 71610-219-20 20 tablet, coated in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Bisacodyl?

Bisacodyl is used to treat constipation. It may also be used to clean out the intestines before a bowel examination/surgery. Bisacodyl is known as a stimulant laxative. It works by increasing the movement of the intestines, helping the stool to come out.

Which are Bisacodyl UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Bisacodyl Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Bisacodyl?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

Patient Education

Bisacodyl


Bisacodyl is used on a short-term basis to treat constipation. It also is used to empty the bowels before surgery and certain medical procedures. Bisacodyl is in a class of medications called stimulant laxatives. It works by increasing activity of the intestines to cause a bowel movement.
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* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".