Acetaminophen Tablet
NDC Package 70518-4783-0

11-digit billing NDC: 70518478300
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Acetaminophen tablets is do not take more than directed (see overdose warning)adults and children 12 years and over:• take 2 tablets every 6 hours while symptoms last• do not take more than 6 tablets in 24 hours, unless directed by a doctor• do not take for more than 10 days unless directed by a doctorchildren under 12 years:ask a doctor. This formulation utilizes a tablet delivery system. Marketed by Remedyrepack Inc., this product is identified by NDC 70518-4783 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
70518-4783-0
Package Description
120 TABLET in 1 BOTTLE, PLASTIC
Product Code
70518-4783
11-Digit Billing Format
70518478300

Clinical Specifications

Proprietary Name
Acetaminophen
Non-Proprietary Name
Acetaminophen
Substance Name
Acetaminophen
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
ACETAMINOPHEN 500 mg/1
Usage Information
Do not take more than directed (see overdose warning)adults and children 12 years and over:• take 2 tablets every 6 hours while symptoms last• do not take more than 6 tablets in 24 hours, unless directed by a doctor• do not take for more than 10 days unless directed by a doctorchildren under 12 years:ask a doctor

Regulatory & Marketing

Labeler Name
Remedyrepack Inc.
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-25-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 70518-4783-0 identifies a specific commercial package of 120 tablet in 1 bottle, plastic of Acetaminophen, a human over the counter drug labeled by Remedyrepack Inc.. This tablet is formulated for oral use and contains acetaminophen as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Remedyrepack Inc. on October 25, 2026. The current certification is valid through December 31, 2027.

How is this Remedyrepack Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70518478300. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
70518-4783-0
11-Digit CMS (5-4-2)
70518-4783-00

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.