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  5. NDC Package Code: 52125-606-19 Finasteride

NDC Package 52125-606-19 Finasteride

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 .

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:
52125-606-19
Package Description:
90 TABLET in 1 VIAL
Product Code:
52125-606
Proprietary Name:
Finasteride
Usage Information:
Finasteride is used to shrink an enlarged prostate (benign prostatic hyperplasia or BPH) in adult men. It may be used alone or taken in combination with other medications to reduce symptoms of BPH and may also reduce the need for surgery. Finasteride may improve symptoms of BPH and provide benefits such as decreased urge to urinate, better urine flow with less straining, less of a feeling that the bladder is not completely emptied, and decreased nighttime urination. This medication works by decreasing the amount of a natural body hormone (DHT) that causes growth of the prostate. Finasteride is not approved for prevention of prostate cancer. It may slightly increase the risk of developing a very serious form of prostate cancer. Talk to your doctor about the benefits and risks. Women and children should not use this medication.
11-Digit NDC Billing Format:
52125060619
Labeler Name:
Remedyrepack Inc.
Sample Package:
No
FDA Application Number:
ANDA090061
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
09-19-2013
End Marketing Date:
09-19-2013
Listing Expiration Date:
09-19-2013
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
52125-606-0230 TABLET in 1 VIAL

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 52125-606-19?

The NDC Packaged Code 52125-606-19 is assigned to a package of 90 tablet in 1 vial of Finasteride, labeled by Remedyrepack Inc.. The product's dosage form is and is administered via form.

Is NDC 52125-606 included in the NDC Directory?

The product was first marketed by Remedyrepack Inc. on September 19, 2013 and its listing in the NDC Directory is set to expire on September 19, 2013 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 52125-606-19?

The 11-digit format is 52125060619. 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
5-3-252125-606-195-4-252125-0606-19