NDC Package 63187-291-04 Acetaminophen And Codeine Phosphate

Solution 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:
63187-291-04
Package Description:
118 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Acetaminophen And Codeine Phosphate
Non-Proprietary Name:
Acetaminophen And Codeine Phosphate
Substance Name:
Acetaminophen; Codeine Phosphate
Usage Information:
Acetaminophen and codeine phosphate oral solution is indicated for the relief of mild to moderate pain.
11-Digit NDC Billing Format:
63187029104
NDC to RxNorm Crosswalk:
  • RxCUI: 993755 - codeine phosphate 12 MG / acetaminophen 120 MG in 5 mL Oral Solution
  • RxCUI: 993755 - acetaminophen 24 MG/ML / codeine phosphate 2.4 MG/ML Oral Solution
  • RxCUI: 993755 - acetaminophen 120 MG / codeine phosphate 12 MG per 5 ML Oral Solution
  • RxCUI: 993755 - acetaminophen 300 MG / codeine phosphate 30 MG per 12.5 ML Oral Solution
  • RxCUI: 993755 - APAP 24 MG/ML / Codeine Phosphate 2.4 MG/ML Oral Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Proficient Rx Lp
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • DEA Schedule:
    Schedule V (CV) Substances
    Sample Package:
    No
    FDA Application Number:
    ANDA087508
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-21-1981
    Listing Expiration Date:
    12-31-2024
    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.

    Frequently Asked Questions

    What is NDC 63187-291-04?

    The NDC Packaged Code 63187-291-04 is assigned to a package of 118 ml in 1 bottle of Acetaminophen And Codeine Phosphate, a human prescription drug labeled by Proficient Rx Lp. The product's dosage form is solution and is administered via oral form.

    Is NDC 63187-291 included in the NDC Directory?

    Yes, Acetaminophen And Codeine Phosphate with product code 63187-291 is active and included in the NDC Directory. The product was first marketed by Proficient Rx Lp on August 21, 1981 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 63187-291-04?

    The 11-digit format is 63187029104. 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
    5-3-263187-291-045-4-263187-0291-04