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  5. NDC Package Code: 69844-044-01 Pramipexole Dihydrochloride

NDC Package 69844-044-01 Pramipexole Dihydrochloride

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
69844-044-01
Package Description:
90 TABLET in 1 BOTTLE
Product Code:
69844-044
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:
69844004401
NDC to RxNorm Crosswalk:
  • RxCUI: 858625 - pramipexole dihydrochloride 0.75 MG Oral Tablet
  • RxCUI: 858625 - pramipexole dihydrochloride 0.75 MG (pramipexole 0.525 MG) Oral Tablet
  • RxCUI: 859040 - pramipexole dihydrochloride 0.25 MG Oral Tablet
  • RxCUI: 859040 - pramipexole dihydrochloride 0.25 MG (pramipexole 0.18 MG) Oral Tablet
  • RxCUI: 859044 - pramipexole dihydrochloride 0.5 MG Oral Tablet
    • Labeler Name:
    Graviti Pharmaceuticals Private Limited
    Sample Package:
    No
    Start Marketing Date:
    04-06-2020
    Listing Expiration Date:
    12-31-2021
    Exclude Flag:
    I
    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 69844-044-01?

    The NDC Packaged Code 69844-044-01 is assigned to a package of 90 tablet in 1 bottle of Pramipexole Dihydrochloride, labeled by Graviti Pharmaceuticals Private Limited. The product's dosage form is and is administered via form.

    Is NDC 69844-044 included in the NDC Directory?

    No, Pramipexole Dihydrochloride with product code 69844-044 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Graviti Pharmaceuticals Private Limited on April 06, 2020 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69844-044-01?

    The 11-digit format is 69844004401. 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
    5-3-269844-044-015-4-269844-0044-01