Acetaminophen Tablet, Film Coated, Extended Release
NDC Package 49035-181-21
Package Information
Acetaminophen tablets is a medication used to treat mild to moderate pain (from headaches, menstrual periods, toothaches, backaches, osteoarthritis, or cold/flu aches and pains) and to reduce fever. This formulation utilizes a tablet, film coated, extended release delivery system. Marketed by Wal-mart Stores Inc, this product is identified by NDC 49035-181 and is authorized under FDA application ANDA211544.
Identification & Billing
- 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
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 49035 - Wal-mart Stores Inc
- 49035-181 - Acetaminophen
- 49035-181-21 - 225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
- 49035-181 - Acetaminophen
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 49035-181-21 identifies a specific commercial package of 225 tablet, film coated, extended release in 1 bottle of Acetaminophen, a human over the counter drug labeled by Wal-mart Stores Inc. This product is billed for "EA" each discreet unit and contains an estimated amount of 225 billable units per package. This tablet, film coated, extended release 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 Wal-mart Stores Inc on October 04, 2019. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
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.
How is this Wal-mart Stores Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 49035018121. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 225 total billable units per package. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.