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  5. NDC Package Code: 68071-2898-3 Sildenafil

NDC Package 68071-2898-3 Sildenafil

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

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
68071-2898-3
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE
Product Code:
68071-2898
Proprietary Name:
Sildenafil
Non-Proprietary Name:
Sildenafil
Substance 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:
68071289803
NDC to RxNorm Crosswalk:
  • RxCUI: 312950 - sildenafil citrate 50 MG Oral Tablet
  • RxCUI: 312950 - sildenafil 50 MG Oral Tablet
  • RxCUI: 312950 - sildenafil 50 MG (as sildenafil citrate) Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Nucare Pharmaceuticals,inc.
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • SILDENAFIL CITRATE 50 mg/1
    • Pharmacologic Class(es):
  • Phosphodiesterase 5 Inhibitor - [EPC] (Established Pharmacologic Class)
  • Phosphodiesterase 5 Inhibitors - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    ANDA202023
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-28-2018
    Listing Expiration Date:
    12-31-2024
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 68071-2898-3?

    The NDC Packaged Code 68071-2898-3 is assigned to a package of 30 tablet, film coated in 1 bottle of Sildenafil, a human prescription drug labeled by Nucare Pharmaceuticals,inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 68071-2898 included in the NDC Directory?

    Yes, Sildenafil with product code 68071-2898 is active and included in the NDC Directory. The product was first marketed by Nucare Pharmaceuticals,inc. on June 28, 2018 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68071-2898-3?

    The 11-digit format is 68071289803. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-168071-2898-35-4-268071-2898-03