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  5. NDC Package Code: 0527-1221-10 Memantine Hydrochloride

NDC Package 0527-1221-10 Memantine Hydrochloride

Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
0527-1221-10
Package Description:
1000 TABLET in 1 BOTTLE, PLASTIC
Product Code:
0527-1221
Proprietary Name:
Memantine Hydrochloride
Non-Proprietary Name:
Memantine Hydrochloride
Substance Name:
Memantine Hydrochloride
Usage Information:
Memantine hydrochloride is indicated for the treatment of moderate to severe dementia of the Alzheimer’s type.
11-Digit NDC Billing Format:
00527122110
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:
    Lannett Company, Inc.
    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):
  • MEMANTINE HYDROCHLORIDE 5 mg/1
    • Pharmacologic Class(es):
  • N-methyl-D-aspartate Receptor Antagonist - [EPC] (Established Pharmacologic Class)
  • NMDA Receptor Antagonists - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    ANDA207236
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-10-2016
    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
    0527-1221-05500 TABLET in 1 BOTTLE, PLASTIC
    0527-1221-0660 TABLET in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0527-1221-10?

    The NDC Packaged Code 0527-1221-10 is assigned to a package of 1000 tablet in 1 bottle, plastic of Memantine Hydrochloride, a human prescription drug labeled by Lannett Company, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 0527-1221 included in the NDC Directory?

    Yes, Memantine Hydrochloride with product code 0527-1221 is active and included in the NDC Directory. The product was first marketed by Lannett Company, Inc. on November 10, 2016 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 0527-1221-10?

    The 11-digit format is 00527122110. 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
    4-4-20527-1221-105-4-200527-1221-10