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  5. NDC Package Code: 57664-228-88 Methylphenidate Hydrochloride

NDC Package 57664-228-88 Methylphenidate 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:
57664-228-88
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
57664-228
Proprietary Name:
Methylphenidate Hydrochloride
Non-Proprietary Name:
Methylphenidate Hydrochloride
Substance Name:
Methylphenidate Hydrochloride
Usage Information:
Methylphenidate hydrochloride tablets are indicated for the treatment of:•Attention Deficit Hyperactivity Disorders (ADHD) in pediatric patients 6 years and older and adults•Narcolepsy
11-Digit NDC Billing Format:
57664022888
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1091150 - methylphenidate HCl 10 MG Oral Tablet
  • RxCUI: 1091150 - methylphenidate hydrochloride 10 MG Oral Tablet
  • RxCUI: 1091392 - methylphenidate HCl 20 MG Oral Tablet
  • RxCUI: 1091392 - methylphenidate hydrochloride 20 MG Oral Tablet
  • RxCUI: 1091497 - methylphenidate HCl 5 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sun Pharmaceutical Industries, 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):
  • METHYLPHENIDATE HYDROCHLORIDE 5 mg/1
    • Pharmacologic Class(es):
  • Central Nervous System Stimulant - [EPC] (Established Pharmacologic Class)
  • Central Nervous System Stimulation - [PE] (Physiologic Effect)
    • DEA Schedule:
    Schedule II (CII) Substances
    Sample Package:
    No
    FDA Application Number:
    ANDA090710
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-16-2013
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    57664-228-08100 TABLET in 1 BOTTLE
    57664-228-13500 TABLET in 1 BOTTLE
    57664-228-181000 TABLET in 1 BOTTLE
    57664-228-8330 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 57664-228-88?

    The NDC Packaged Code 57664-228-88 is assigned to a package of 100 tablet in 1 bottle of Methylphenidate Hydrochloride, a human prescription drug labeled by Sun Pharmaceutical Industries, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 57664-228 included in the NDC Directory?

    Yes, Methylphenidate Hydrochloride with product code 57664-228 is active and included in the NDC Directory. The product was first marketed by Sun Pharmaceutical Industries, Inc. on August 16, 2013 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 57664-228-88?

    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 100.

    What is the 11-digit format for NDC 57664-228-88?

    The 11-digit format is 57664022888. 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
    5-3-257664-228-885-4-257664-0228-88