NDC Package 0832-1113-60 Memantine Hydrochloride

Tablet, Film Coated 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:
0832-1113-60
Package Description:
60 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Memantine Hydrochloride
Non-Proprietary Name:
Memantine Hydrochloride
Substance Name:
Memantine Hydrochloride
Usage Information:
Memantine Hydrochloride Tablets are indicated for the treatment of moderate to severe dementia of the Alzheimer's type.
11-Digit NDC Billing Format:
00832111360
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
60 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 996561 - memantine HCl 10 MG Oral Tablet
  • RxCUI: 996561 - memantine hydrochloride 10 MG Oral Tablet
  • RxCUI: 996571 - memantine HCl 5 MG Oral Tablet
  • RxCUI: 996571 - memantine hydrochloride 5 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Upsher-smith Laboratories, Llc
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA090043
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-31-2015
    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 0832-1113-60?

    The NDC Packaged Code 0832-1113-60 is assigned to a package of 60 tablet, film coated in 1 bottle of Memantine Hydrochloride, a human prescription drug labeled by Upsher-smith Laboratories, Llc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 0832-1113 included in the NDC Directory?

    Yes, Memantine Hydrochloride with product code 0832-1113 is active and included in the NDC Directory. The product was first marketed by Upsher-smith Laboratories, Llc on July 31, 2015 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 0832-1113-60?

    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 60.

    What is the 11-digit format for NDC 0832-1113-60?

    The 11-digit format is 00832111360. 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 4-4-2 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
    4-4-20832-1113-605-4-200832-1113-60