NDC Package 17856-8100-3 Sildenafil Citrate

View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
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:

17856-8100-3

Package Description:

200 POUCH in 1 BOX / 3 TABLET, FILM COATED in 1 POUCH

Product Code:

17856-8100

Proprietary Name:

Sildenafil Citrate

Usage Information:

Sildenafil is used to treat high blood pressure in the lungs (pulmonary hypertension). It works by relaxing and widening the blood vessels in your lungs which allows the blood to flow more easily. Decreasing high blood pressure in the lungs allows your heart and lungs to work better and improves your ability to exercise. This medication is not recommended for use in children. Discuss the risks and benefits of this medication with the doctor.

11-Digit NDC Billing Format:

17856810003

NDC to RxNorm Crosswalk:

RxCUI: 577033 - sildenafil citrate 20 MG Oral Tablet

RxCUI: 577033 - sildenafil 20 MG Oral Tablet

RxCUI: 577033 - sildenafil 20 MG (as sildenafil citrate) Oral Tablet

Labeler Name:

Atlantic Biologicals Corp.

Sample Package:

Start Marketing Date:

07-29-2019

Listing Expiration Date:

12-31-2022

Exclude Flag:

Code Structure:

17856 - Atlantic Biologicals Corp.
- 17856-8100 - Sildenafil Citrate
  - 17856-8100-3 - 200 POUCH in 1 BOX / 3 TABLET, FILM COATED in 1 POUCH

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 Code	Package Description
17856-8100-1	200 POUCH in 1 BOX / 1 TABLET, FILM COATED in 1 POUCH
17856-8100-2	200 POUCH in 1 BOX / 2 TABLET, FILM COATED in 1 POUCH
17856-8100-4	200 POUCH in 1 BOX / 4 TABLET, FILM COATED in 1 POUCH
17856-8100-5	200 POUCH in 1 BOX / 5 TABLET, FILM COATED in 1 POUCH

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 17856-8100-3?

The NDC Packaged Code 17856-8100-3 is assigned to a package of 200 pouch in 1 box / 3 tablet, film coated in 1 pouch of Sildenafil Citrate, labeled by Atlantic Biologicals Corp.. The product's dosage form is and is administered via form.

Is NDC 17856-8100 included in the NDC Directory?

No, Sildenafil Citrate with product code 17856-8100 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Atlantic Biologicals Corp. on July 29, 2019 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 17856-8100-3?

The 11-digit format is 17856810003. 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 5-4-1 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-4-1	17856-8100-3	5-4-2	17856-8100-03

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