NDC Package 67877-648-11 Sildenafil Citrate

Powder, For Suspension Oral - View Billable Units, 11-Digit Format, RxNorm

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:
67877-648-11
Package Description:
1 BOTTLE, GLASS in 1 CARTON / 112 mL in 1 BOTTLE, GLASS
Product Code:
Proprietary Name:
Sildenafil Citrate
Non-Proprietary Name:
Sildenafil Citrate
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:
67877064811
NDC to RxNorm Crosswalk:
  • RxCUI: 1307427 - sildenafil 10 MG in 1 mL Oral Suspension
  • RxCUI: 1307427 - sildenafil 10 MG/ML Oral Suspension
  • RxCUI: 1307427 - sildenafil (as sildenafil citrate) 10 MG/ML Powder for Oral Suspension
  • RxCUI: 1307427 - sildenafil 10 MG per 1 ML Oral Suspension
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Ascend Laboratories, Llc
    Dosage Form:
    Powder, For Suspension - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a suspension (a liquid preparation containing the solid particles dispersed in the liquid vehicle).
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA212440
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-29-2019
    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 67877-648-11?

    The NDC Packaged Code 67877-648-11 is assigned to a package of 1 bottle, glass in 1 carton / 112 ml in 1 bottle, glass of Sildenafil Citrate, a human prescription drug labeled by Ascend Laboratories, Llc. The product's dosage form is powder, for suspension and is administered via oral form.

    Is NDC 67877-648 included in the NDC Directory?

    Yes, Sildenafil Citrate with product code 67877-648 is active and included in the NDC Directory. The product was first marketed by Ascend Laboratories, Llc on November 29, 2019 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 67877-648-11?

    The 11-digit format is 67877064811. 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
    5-3-267877-648-115-4-267877-0648-11