NDC Package 58602-730-41 Acetaminophen

Tablet, Extended Release 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:
58602-730-41
Package Description:
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Code:
Proprietary Name:
Acetaminophen
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:
58602073041
NDC to RxNorm Crosswalk:
  • RxCUI: 1148399 - acetaminophen 650 MG 8HR Extended Release Oral Tablet
  • RxCUI: 1148399 - 8 HR acetaminophen 650 MG Extended Release Oral Tablet
  • RxCUI: 1148399 - 8 HR APAP 650 MG Extended Release Oral Tablet
  • RxCUI: 1148399 - acetaminophen 650 MG 8 HR Extended Release Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Aurohealth Llc
    Dosage Form:
    Tablet, Extended Release - A solid dosage form containing a drug which allows at least a reduction in dosing frequency as compared to that drug presented in conventional dosage form.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA207229
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-09-2016
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    58602-730-071 BOTTLE in 1 CARTON / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE
    58602-730-141 BOTTLE in 1 CARTON / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE
    58602-730-211 BOTTLE in 1 CARTON / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE
    58602-730-281 BOTTLE in 1 CARTON / 225 TABLET, EXTENDED RELEASE in 1 BOTTLE
    58602-730-29150 TABLET, EXTENDED RELEASE in 1 BOTTLE
    58602-730-34200 TABLET, EXTENDED RELEASE in 1 BOTTLE
    58602-730-35225 TABLET, EXTENDED RELEASE in 1 BOTTLE
    58602-730-361 BOTTLE in 1 CARTON / 250 TABLET, EXTENDED RELEASE in 1 BOTTLE
    58602-730-40500 TABLET, EXTENDED RELEASE in 1 BOTTLE
    58602-730-44400 TABLET, EXTENDED RELEASE in 1 BOTTLE
    58602-730-67290 TABLET, EXTENDED RELEASE in 1 BOTTLE
    58602-730-76325 TABLET, EXTENDED RELEASE in 1 BOTTLE
    58602-730-94100 TABLET, EXTENDED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 58602-730-41?

    The NDC Packaged Code 58602-730-41 is assigned to a package of 1000 tablet, extended release in 1 bottle of Acetaminophen, a human over the counter drug labeled by Aurohealth Llc. The product's dosage form is tablet, extended release and is administered via oral form.

    Is NDC 58602-730 included in the NDC Directory?

    Yes, Acetaminophen with product code 58602-730 is active and included in the NDC Directory. The product was first marketed by Aurohealth Llc on November 09, 2016 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 11-digit format for NDC 58602-730-41?

    The 11-digit format is 58602073041. 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
    5-3-258602-730-415-4-258602-0730-41