Acetaminophen And Codeine Phosphate Tablet
NDC Package 49999-060-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

Acetaminophen And Codeine Phosphate tablets are indicated for the relief of mild to moderately severe pain. This formulation utilizes a tablet delivery system. Marketed by Quality Care Products, Llc, this product is identified by NDC 49999-060 and is authorized under FDA application ANDA040419.

Identification & Billing

NDC Package Code
49999-060-01
Package Description
120 TABLET in 1 BOTTLE
Product Code
49999-060
11-Digit Billing Format
49999006001
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
120 EA
RxNorm Crosswalk
  • RxCUI: 993781 - codeine phosphate 30 MG / acetaminophen 300 MG Oral Tablet
  • RxCUI: 993781 - acetaminophen 300 MG / codeine phosphate 30 MG Oral Tablet
  • RxCUI: 993781 - APAP 300 MG / codeine phosphate 30 MG Oral Tablet

Clinical Specifications

Proprietary Name
Acetaminophen And Codeine Phosphate
Non-Proprietary Name
Acetaminophen And Codeine Phosphate
Substance Name
Acetaminophen; Codeine Phosphate
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)
Pharmacologic Class
Usage Information
Acetaminophen and codeine phosphate tablets are indicated for the relief of mild to moderately severe pain.
DEA Schedule
Schedule III (CIII) Substances

Regulatory & Marketing

Labeler Name
Quality Care Products, Llc
Product Type
Human Prescription Drug
FDA Application #
ANDA040419
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
09-14-2011
End Marketing Date
09-30-2026
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (49999-060). Click a package code to view its specific billing and regulatory data.

49999-060-00
100 TABLET in 1 BOTTLE
49999-060-06
6 TABLET in 1 BOTTLE
49999-060-10
10 TABLET in 1 BOTTLE
49999-060-12
12 TABLET in 1 BOTTLE
49999-060-15
15 TABLET in 1 BOTTLE
49999-060-20
20 TABLET in 1 BOTTLE
49999-060-24
24 TABLET in 1 BOTTLE
49999-060-30
30 TABLET in 1 BOTTLE
49999-060-50
50 TABLET in 1 BOTTLE
49999-060-60
60 TABLET in 1 BOTTLE
49999-060-90
90 TABLET in 1 BOTTLE

* 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 49999-060-01 identifies a specific commercial package of 120 tablet in 1 bottle of Acetaminophen And Codeine Phosphate, a human prescription drug labeled by Quality Care Products, Llc. This product is billed for "EA" each discreet unit and contains an estimated amount of 120 billable units per package. This tablet is formulated for oral use and contains acetaminophen; codeine phosphate 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 Quality Care Products, Llc on September 14, 2011.

How is this Quality Care Products, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49999006001. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 120 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:

10-Digit Format (5-3-2)
49999-060-01
11-Digit CMS (5-4-2)
49999-0060-01

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