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  5. NDC Package Code: 60687-416-21 Sildenafil

NDC Package 60687-416-21 Sildenafil

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
60687-416-21
Package Description:
30 BLISTER PACK in 1 BOX, UNIT-DOSE / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-416-11)
Product Code:
60687-416
Proprietary Name:
Sildenafil
Usage Information:
Sildenafil tablets are indicated for the treatment of pulmonary arterial hypertension (WHO Group I) in adults to improve exercise ability and delay clinical worsening. The delay in clinical worsening was demonstrated when sildenafil tablets were added to background epoprostenol therapy [ see Clinical Studies ( 14) ]. Studies establishing effectiveness were short-term (12 to 16 weeks), and included predominately patients with New York Heart Association (NYHA) Functional Class II-III symptoms and idiopathic etiology (71%) or associated with connective tissue disease (CTD) (25%).Limitation of Use: Adding sildenafil to bosentan therapy does not result in any beneficial effect on exercise capacity [ see Clinical Studies ( 14) ].
11-Digit NDC Billing Format:
60687041621
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
30 EA
NDC to RxNorm Crosswalk:
Labeler Name:
American Health Packaging
Sample Package:
No
FDA Application Number:
ANDA203814
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
02-19-2019
End Marketing Date:
06-30-2025
Listing Expiration Date:
06-30-2025
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.

Frequently Asked Questions

What is NDC 60687-416-21?

The NDC Packaged Code 60687-416-21 is assigned to a package of 30 blister pack in 1 box, unit-dose / 1 tablet, film coated in 1 blister pack (60687-416-11) of Sildenafil, labeled by American Health Packaging. The product's dosage form is and is administered via form.

Is NDC 60687-416 included in the NDC Directory?

No, Sildenafil with product code 60687-416 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by American Health Packaging on February 19, 2019 and its listing in the NDC Directory is set to expire on June 30, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 60687-416-21?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 30.

What is the 11-digit format for NDC 60687-416-21?

The 11-digit format is 60687041621. 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
5-3-260687-416-215-4-260687-0416-21