NDC Package 70954-005-30 Oxybutynin Chloride

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:
70954-005-30
Package Description:
1000 TABLET 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:
70954000530
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1000 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 863664 - oxyBUTYnin chloride 5 MG Oral Tablet
  • RxCUI: 863664 - oxybutynin chloride 5 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Novitium Pharma Llc
    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):
    Sample Package:
    No
    FDA Application Number:
    ANDA209823
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-15-2017
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    70954-005-10100 TABLET in 1 BOTTLE
    70954-005-20500 TABLET in 1 BOTTLE
    70954-005-50100 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK (70954-005-40)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70954-005-30?

    The NDC Packaged Code 70954-005-30 is assigned to a package of 1000 tablet in 1 bottle of Oxybutynin Chloride, a human prescription drug labeled by Novitium Pharma Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 70954-005 included in the NDC Directory?

    Yes, Oxybutynin Chloride with product code 70954-005 is active and included in the NDC Directory. The product was first marketed by Novitium Pharma Llc on November 15, 2017 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 NDC billing unit for package 70954-005-30?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1000.

    What is the 11-digit format for NDC 70954-005-30?

    The 11-digit format is 70954000530. 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
    5-3-270954-005-305-4-270954-0005-30