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  5. NDC Package Code: 33342-032-06 Pramipexole Dihydrochloride

NDC Package 33342-032-06 Pramipexole Dihydrochloride

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
33342-032-06
Package Description:
30 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK
Product Code:
33342-032
Proprietary Name:
Pramipexole Dihydrochloride
Usage Information:
Pramipexole is used alone or with other medications to treat Parkinson's disease. It can improve your ability to move and decrease shakiness (tremor), stiffness, slowed movement, and unsteadiness. It may also decrease the number of episodes of not being able to move ("on-off syndrome"). This medication is also used to treat a certain medical condition (restless legs syndrome - RLS) that causes an unusual urge to move the legs. Symptoms usually occur at night along with uncomfortable/unpleasant feelings in the legs. This medication can decrease these symptoms and thereby improve sleep. Pramipexole is a dopamine agonist that works by helping to restore the balance of a certain natural substance (dopamine) in the brain.
11-Digit NDC Billing Format:
33342003206
Labeler Name:
Macleods Pharmaceuticals Limited
Sample Package:
No
FDA Application Number:
ANDA202164
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
09-21-2012
End Marketing Date:
05-29-2020
Listing Expiration Date:
05-29-2020
Exclude Flag:
D
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
33342-032-1090 TABLET in 1 BOTTLE
33342-032-12100 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK
33342-032-15500 TABLET in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 33342-032-06?

The NDC Packaged Code 33342-032-06 is assigned to a package of 30 blister pack in 1 carton / 1 tablet in 1 blister pack of Pramipexole Dihydrochloride, labeled by Macleods Pharmaceuticals Limited. The product's dosage form is and is administered via form.

Is NDC 33342-032 included in the NDC Directory?

No, Pramipexole Dihydrochloride with product code 33342-032 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Macleods Pharmaceuticals Limited on September 21, 2012 and its listing in the NDC Directory is set to expire on May 29, 2020 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 33342-032-06?

The 11-digit format is 33342003206. 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
5-3-233342-032-065-4-233342-0032-06