NDC Package 73057-350-08 Pharbetol

Acetaminophen 500mg Tablet, Coated 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:
73057-350-08
Package Description:
100 TABLET, COATED in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Pharbetol
Non-Proprietary Name:
Acetaminophen 500mg
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:
73057035008
NDC to RxNorm Crosswalk:
  • RxCUI: 1293942 - Pharbetol 500 MG Oral Tablet
  • RxCUI: 1293942 - acetaminophen 500 MG Oral Tablet [Pharbetol]
  • RxCUI: 1293942 - APAP 500 MG Oral Tablet [Pharbetol]
  • RxCUI: 198440 - acetaminophen 500 MG Oral Tablet
  • RxCUI: 198440 - APAP 500 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Ulai Health Llc
    Dosage Form:
    Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    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:
    07-08-2019
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    73057-350-111000 TABLET, COATED in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 73057-350-08?

    The NDC Packaged Code 73057-350-08 is assigned to a package of 100 tablet, coated in 1 bottle, plastic of Pharbetol, a human over the counter drug labeled by Ulai Health Llc. The product's dosage form is tablet, coated and is administered via oral form.

    Is NDC 73057-350 included in the NDC Directory?

    Yes, Pharbetol with product code 73057-350 is active and included in the NDC Directory. The product was first marketed by Ulai Health Llc on July 08, 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 73057-350-08?

    The 11-digit format is 73057035008. 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
    5-3-273057-350-085-4-273057-0350-08