NDC Package 70954-168-10 Sildenafil

Sildenafil Citrate 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:
70954-168-10
Package Description:
1 BOTTLE in 1 CARTON / 112 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Sildenafil
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:
70954016810
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
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:
    Ani Pharmaceuticals, Inc.
    Dosage Form:
    For Suspension - A product, usually a solid, intended for suspension prior to administration.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA212260
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    05-31-2019
    Listing Expiration Date:
    12-31-2025
    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 70954-168-10?

    The NDC Packaged Code 70954-168-10 is assigned to a package of 1 bottle in 1 carton / 112 ml in 1 bottle of Sildenafil, a human prescription drug labeled by Ani Pharmaceuticals, Inc.. The product's dosage form is for suspension and is administered via oral form.

    Is NDC 70954-168 included in the NDC Directory?

    Yes, Sildenafil with product code 70954-168 is active and included in the NDC Directory. The product was first marketed by Ani Pharmaceuticals, Inc. on May 31, 2019 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 70954-168-10?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 70954-168-10?

    The 11-digit format is 70954016810. 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
    5-3-270954-168-105-4-270954-0168-10