NDC Package 65580-531-01 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 inactivated by the FDA.

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:

65580-531-01

Package Description:

100 TABLET in 1 BOTTLE

Product Code:

65580-531

Proprietary Name:

Methylphenidate Hydrochloride

Usage Information:

Marked anxiety, tension, and agitation are contraindications to methylphenidate, since the drug may aggravate these symptoms. Methylphenidate 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 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:

65580053101

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

Labeler Name:

Upstate Pharma, Llc

Sample Package:

Start Marketing Date:

11-01-2014

Listing Expiration Date:

12-31-2018

Exclude Flag:

Code Structure:

65580 - Upstate Pharma, Llc
- 65580-531 - Methylphenidate Hydrochloride
  - 65580-531-01 - 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 65580-531-01?

The NDC Packaged Code 65580-531-01 is assigned to a package of 100 tablet in 1 bottle of Methylphenidate Hydrochloride, labeled by Upstate Pharma, Llc. The product's dosage form is and is administered via form.

Is NDC 65580-531 included in the NDC Directory?

No, Methylphenidate Hydrochloride with product code 65580-531 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Upstate Pharma, Llc on November 01, 2014 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 65580-531-01?

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 65580-531-01?

The 11-digit format is 65580053101. 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	65580-531-01	5-4-2	65580-0531-01

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