NDC Package 0615-8552-39 Pramipexole Dihydrochloride

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

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:
0615-8552-39
Package Description:
30 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Pramipexole Dihydrochloride
Non-Proprietary Name:
Pramipexole Dihydrochloride
Substance 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:
00615855239
NDC to RxNorm Crosswalk:
  • 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
  • RxCUI: 859044 - pramipexole dihydrochloride 0.5 MG (pramipexole 0.35 MG) Oral Tablet
Product Type:
Human Prescription Drug
Labeler Name:
Ncs Healthcare Of Ky, Llc Dba Vangard Labs
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.
Sample Package:
No
FDA Application Number:
ANDA090781
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
10-08-2010
Listing Expiration Date:
12-31-2025
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.

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Frequently Asked Questions

What is NDC 0615-8552-39?

The NDC Packaged Code 0615-8552-39 is assigned to a package of 30 tablet in 1 blister pack of Pramipexole Dihydrochloride, a human prescription drug labeled by Ncs Healthcare Of Ky, Llc Dba Vangard Labs. The product's dosage form is tablet and is administered via oral form.

Is NDC 0615-8552 included in the NDC Directory?

Yes, Pramipexole Dihydrochloride with product code 0615-8552 is active and included in the NDC Directory. The product was first marketed by Ncs Healthcare Of Ky, Llc Dba Vangard Labs on October 08, 2010 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0615-8552-39?

The 11-digit format is 00615855239. 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 4-4-2 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
4-4-20615-8552-395-4-200615-8552-39