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  5. NDC Package Code: 16729-479-01 Methylphenidate Hydrochloride

NDC Package 16729-479-01 Methylphenidate Hydrochloride

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

Table of Contents

    1. Package Information
    2. 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:
16729-479-01
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
16729-479
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 adultsNarcolepsy
11-Digit NDC Billing Format:
16729047901
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:
    Accord Healthcare, 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 10 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:
    ANDA213936
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-17-2020
    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 16729-479-01?

    The NDC Packaged Code 16729-479-01 is assigned to a package of 100 tablet in 1 bottle of Methylphenidate Hydrochloride, a human prescription drug labeled by Accord Healthcare, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 16729-479 included in the NDC Directory?

    Yes, Methylphenidate Hydrochloride with product code 16729-479 is active and included in the NDC Directory. The product was first marketed by Accord Healthcare, Inc. on December 17, 2020 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 16729-479-01?

    The 11-digit format is 16729047901. 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
    5-3-216729-479-015-4-216729-0479-01