Memantine Hydrochloride Tablet, Film Coated
NDC Package 55111-596-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Memantine Hydrochloride tablets are indicated for the treatment of moderate to severe dementia of the Alzheimer’s type. This formulation utilizes a tablet, film coated delivery system. Marketed by Dr. Reddys Laboratories Limited, this product is identified by NDC 55111-596 and is authorized under FDA application ANDA090048.

Identification & Billing

NDC Package Code
55111-596-01
Package Description
100 TABLET, FILM COATED in 1 BOTTLE
Product Code
11-Digit Billing Format
55111059601
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Memantine Hydrochloride
Non-Proprietary Name
Memantine Hydrochloride
Substance Name
Memantine Hydrochloride
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
Memantine hydrochloride tablets are indicated for the treatment of moderate to severe dementia of the Alzheimer’s type.  

Regulatory & Marketing

Labeler Name
Dr. Reddys Laboratories Limited
Product Type
Human Prescription Drug
FDA Application #
ANDA090048
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
07-11-2015
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (55111-596). Click a package code to view its specific billing and regulatory data.

500 TABLET, FILM COATED in 1 BOTTLE
30 TABLET, FILM COATED in 1 BOTTLE
60 TABLET, FILM COATED in 1 BOTTLE
10 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK
1 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 55111-596-01 identifies a specific commercial package of 100 tablet, film coated in 1 bottle of Memantine Hydrochloride, a human prescription drug labeled by Dr. Reddys Laboratories Limited. This tablet, film coated is formulated for oral use and contains memantine hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Dr. Reddys Laboratories Limited on July 11, 2015. The current certification is valid through December 31, 2026.

How is this Dr. Reddys Laboratories Limited product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 55111059601. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
55111-596-01
11-Digit CMS (5-4-2)
55111-0596-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.