NDC Package 57237-049-60 Galantamine

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:
57237-049-60
Package Description:
60 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Galantamine
Non-Proprietary Name:
Galantamine
Substance Name:
Galantamine Hydrobromide
Usage Information:
Galantamine tablets are indicated for the treatment of mild to moderate dementia of the Alzheimer’s type.
11-Digit NDC Billing Format:
57237004960
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: 310436 - galantamine HBr 4 MG Oral Tablet
  • RxCUI: 310436 - galantamine 4 MG Oral Tablet
  • RxCUI: 310436 - galantamine 4 MG (as galantamine hydrobromide 5.126 MG) Oral Tablet
  • RxCUI: 310437 - galantamine HBr 8 MG Oral Tablet
  • RxCUI: 310437 - galantamine 8 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Rising Pharma Holdings, Inc.
    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:
    ANDA090957
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-29-2011
    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.

    Frequently Asked Questions

    What is NDC 57237-049-60?

    The NDC Packaged Code 57237-049-60 is assigned to a package of 60 tablet, film coated in 1 bottle of Galantamine, a human prescription drug labeled by Rising Pharma Holdings, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 57237-049 included in the NDC Directory?

    Yes, Galantamine with product code 57237-049 is active and included in the NDC Directory. The product was first marketed by Rising Pharma Holdings, Inc. on March 29, 2011 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 NDC billing unit for package 57237-049-60?

    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 57237-049-60?

    The 11-digit format is 57237004960. 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
    5-3-257237-049-605-4-257237-0049-60