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  5. NDC Package Code: 70954-652-20 Finasteride And Tadalafil

NDC Package 70954-652-20 Finasteride And Tadalafil

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:
70954-652-20
Package Description:
90 CAPSULE in 1 BOTTLE
Product Code:
70954-652
Proprietary Name:
Finasteride And Tadalafil
Usage Information:
Finasteride and tadalafil is indicated to initiate treatment of the signs and symptoms of benign prostatic hyperplasia (BPH) in men with an enlarged prostate for up to 26 weeks.Limitations of UseFinasteride and tadalafil is not recommended for more than 26 weeks because the incremental benefit of tadalafil decreases from 4 weeks until 26 weeks, and the incremental benefit beyond 26 weeks is unknown [see Clinical Studies (14)].
11-Digit NDC Billing Format:
70954065220
Labeler Name:
Ani Pharmaceuticals, Inc.
Sample Package:
No
FDA Application Number:
ANDA218499
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
03-24-2025
End Marketing Date:
03-24-2025
Listing Expiration Date:
03-24-2025
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
70954-652-1030 CAPSULE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70954-652-20?

The NDC Packaged Code 70954-652-20 is assigned to a package of 90 capsule in 1 bottle of Finasteride And Tadalafil, labeled by Ani Pharmaceuticals, Inc.. The product's dosage form is and is administered via form.

Is NDC 70954-652 included in the NDC Directory?

No, Finasteride And Tadalafil with product code 70954-652 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Ani Pharmaceuticals, Inc. on March 24, 2025 and its listing in the NDC Directory is set to expire on March 24, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70954-652-20?

The 11-digit format is 70954065220. 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
5-3-270954-652-205-4-270954-0652-20