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  5. NDC Package Code: 31722-906-10 Pramipexole

NDC Package 31722-906-10 Pramipexole

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
31722-906-10
Package Description:
1000 TABLET in 1 BOTTLE
Product Code:
31722-906
Proprietary Name:
Pramipexole
Non-Proprietary Name:
Pramipexole
Substance Name:
Pramipexole Dihydrochloride
Usage Information:
None.
11-Digit NDC Billing Format:
31722090610
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: 859033 - pramipexole dihydrochloride 0.125 MG Oral Tablet
  • RxCUI: 859033 - pramipexole dihydrochloride 0.125 MG (pramipexole 0.088 MG) Oral Tablet
  • RxCUI: 859040 - pramipexole dihydrochloride 0.25 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Camber Pharmaceuticals, 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):
  • PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1
    • Pharmacologic Class(es):
  • Dopamine Agonists - [MoA] (Mechanism of Action)
  • Nonergot Dopamine Agonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA203855
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-01-2015
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    31722-906-05500 TABLET in 1 BOTTLE
    31722-906-9090 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 31722-906-10?

    The NDC Packaged Code 31722-906-10 is assigned to a package of 1000 tablet in 1 bottle of Pramipexole, a human prescription drug labeled by Camber Pharmaceuticals, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 31722-906 included in the NDC Directory?

    Yes, Pramipexole with product code 31722-906 is active and included in the NDC Directory. The product was first marketed by Camber Pharmaceuticals, Inc. on August 01, 2015 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 31722-906-10?

    The 11-digit format is 31722090610. 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
    5-3-231722-906-105-4-231722-0906-10