NDC Package 16714-823-01 Methylphenidate Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Package Information
Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:

16714-823-01

Package Description:

100 TABLET in 1 BOTTLE

Product Code:

16714-823

Proprietary Name:

Methylphenidate Hydrochloride

Usage Information:

Marked anxiety, tension, and agitation are contraindications to methylphenidate hydrochloride, since the drug may aggravate these symptoms. Methylphenidate hydrochloride is contraindicated also in patients known to be hypersensitive to the drug, in patients with glaucoma, and in patients with motor tics or with a family history or diagnosis of Tourette’s syndrome.Methylphenidate hydrochloride is contraindicated during treatment with monoamine oxidase inhibitors, and also within a minimum of 14 days following discontinuation of a monoamine oxidase inhibitor (hypertensive crises may result).

11-Digit NDC Billing Format:

16714082301

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

100 EA

Labeler Name:

Northstar Rx Llc

Sample Package:

FDA Application Number:

ANDA207416

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

10-01-2015

End Marketing Date:

04-30-2024

Listing Expiration Date:

04-30-2024

Exclude Flag:

Code Structure:

16714 - Northstar Rx Llc
- 16714-823 - Methylphenidate Hydrochloride
  - 16714-823-01 - 100 TABLET in 1 BOTTLE

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 16714-823-01?

The NDC Packaged Code 16714-823-01 is assigned to a package of 100 tablet in 1 bottle of Methylphenidate Hydrochloride, labeled by Northstar Rx Llc. The product's dosage form is and is administered via form.

Is NDC 16714-823 included in the NDC Directory?

No, Methylphenidate Hydrochloride with product code 16714-823 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Northstar Rx Llc on October 01, 2015 and its listing in the NDC Directory is set to expire on April 30, 2024 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 16714-823-01?

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 16714-823-01?

The 11-digit format is 16714082301. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	16714-823-01	5-4-2	16714-0823-01

Table of Contents