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  5. NDC Package Code: 51672-5320-8 Feverall

NDC Package 51672-5320-8 Feverall

Acetaminophen Suspension 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:
51672-5320-8
Package Description:
1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Product Code:
51672-5320
Proprietary Name:
Feverall
Non-Proprietary Name:
Acetaminophen
Substance Name:
Acetaminophen
Usage Information:
This drug is used to treat mild to moderate pain (from headaches, menstrual periods, toothaches, backaches, osteoarthritis, or cold/flu aches and pains) and to reduce fever.
11-Digit NDC Billing Format:
51672532008
NDC to RxNorm Crosswalk:
  • RxCUI: 2639351 - Feverall Children's 160 MG in 5 mL Oral Suspension
  • RxCUI: 2639351 - acetaminophen 32 MG/ML Oral Suspension [Feverall]
  • RxCUI: 2639351 - APAP 32 MG/ML Oral Suspension [Feverall]
  • RxCUI: 2639351 - Feverall 32 MG/ML Oral Suspension
  • RxCUI: 2639351 - Feverall Children's 160 MG per 5 ML Oral Suspension
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Taro Pharmaceuticals U.s.a., Inc.
    Dosage Form:
    Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETAMINOPHEN 160 mg/5mL
    • Sample Package:
    No
    FDA Application Number:
    part343
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    06-01-2023
    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 51672-5320-8?

    The NDC Packaged Code 51672-5320-8 is assigned to a package of 1 bottle in 1 carton / 118 ml in 1 bottle of Feverall, a human over the counter drug labeled by Taro Pharmaceuticals U.s.a., Inc.. The product's dosage form is suspension and is administered via oral form.

    Is NDC 51672-5320 included in the NDC Directory?

    Yes, Feverall with product code 51672-5320 is active and included in the NDC Directory. The product was first marketed by Taro Pharmaceuticals U.s.a., Inc. on June 01, 2023 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 51672-5320-8?

    The 11-digit format is 51672532008. 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
    5-4-151672-5320-85-4-251672-5320-08