Combogesic Tablet, Film Coated
NDC Package 72260-129-01
Package Information
Combogesic (acetaminophen and ibuprofen) tablets is cOMBOGESIC and is indicated in adults for the short-term management of mild to moderate acute pain. This formulation utilizes a tablet, film coated delivery system. Marketed by Aft Pharmaceuticals Us, Inc., this product is identified by NDC 72260-129 and is authorized under FDA application NDA209471.
Identification & Billing
- RxCUI: 2675760 - acetaminophen 325 MG / ibuprofen 97.5 MG Oral Tablet
- RxCUI: 2675760 - APAP 325 MG / ibuprofen 97.5 MG Oral Tablet
- RxCUI: 2675765 - combogesic 325 MG / 97.5 MG Oral Tablet
- RxCUI: 2675765 - acetaminophen 325 MG / ibuprofen 97.5 MG Oral Tablet [Combogesic]
- RxCUI: 2675765 - APAP 325 MG / ibuprofen 97.5 MG Oral Tablet [Combogesic]
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 72260 - Aft Pharmaceuticals Us, Inc.
- 72260-129 - Combogesic
- 72260-129-01 - 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
- 72260-129 - Combogesic
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 72260-129-01 identifies a specific commercial package of 250 tablet, film coated in 1 bottle, plastic of Combogesic, a human prescription drug labeled by Aft Pharmaceuticals Us, Inc.. This product is billed for "EA" each discreet unit and contains an estimated amount of 250 billable units per package. This tablet, film coated is formulated for oral use and contains acetaminophen; ibuprofen 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 Aft Pharmaceuticals Us, Inc. on January 06, 2025. The current certification is valid through December 31, 2026.
How is this Aft Pharmaceuticals Us, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 72260012901. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 250 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.