NDC Package 71335-1690-3 Oxybutynin Chloride

Tablet, Extended Release 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:
71335-1690-3
Package Description:
90 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Code:
Proprietary Name:
Oxybutynin Chloride
Non-Proprietary Name:
Oxybutynin Chloride
Substance Name:
Oxybutynin Chloride
Usage Information:
Oxybutynin is used to treat certain bladder and urinary conditions (e.g., overactive bladder). It relaxes the muscles in the bladder to help decrease problems of urgency and frequent urination. Oxybutynin belongs to a class of drugs known as antispasmodics. The manufacturer does not recommend using this medication in children younger than 5 years of age.
11-Digit NDC Billing Format:
71335169003
NDC to RxNorm Crosswalk:
  • RxCUI: 863619 - oxyBUTYnin chloride 10 MG 24HR Extended Release Oral Tablet
  • RxCUI: 863619 - 24 HR oxybutynin chloride 10 MG Extended Release Oral Tablet
  • RxCUI: 863619 - oxybutynin chloride 10 MG 24 HR Extended Release Oral Tablet
Product Type:
Human Prescription Drug
Labeler Name:
Bryant Ranch Prepack
Dosage Form:
Tablet, Extended Release - A solid dosage form containing a drug which allows at least a reduction in dosing frequency as compared to that drug presented in conventional dosage form.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Sample Package:
No
FDA Application Number:
ANDA211655
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
02-28-2019
Listing Expiration Date:
12-31-2025
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
71335-1690-130 TABLET, EXTENDED RELEASE in 1 BOTTLE
71335-1690-218 TABLET, EXTENDED RELEASE in 1 BOTTLE
71335-1690-460 TABLET, EXTENDED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 71335-1690-3?

The NDC Packaged Code 71335-1690-3 is assigned to a package of 90 tablet, extended release in 1 bottle of Oxybutynin Chloride, a human prescription drug labeled by Bryant Ranch Prepack. The product's dosage form is tablet, extended release and is administered via oral form.

Is NDC 71335-1690 included in the NDC Directory?

Yes, Oxybutynin Chloride with product code 71335-1690 is active and included in the NDC Directory. The product was first marketed by Bryant Ranch Prepack on February 28, 2019 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 71335-1690-3?

The 11-digit format is 71335169003. 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 5-4-1 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
5-4-171335-1690-35-4-271335-1690-03