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  5. NDC Package Code: 0363-6199-23 Dual Back Pain Reliever

NDC Package 0363-6199-23 Dual Back Pain Reliever

Acetaminophen,Ibuprofen Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
0363-6199-23
Package Description:
1 BOTTLE in 1 CARTON / 72 TABLET, FILM COATED in 1 BOTTLE
Product Code:
0363-6199
Proprietary Name:
Dual Back Pain Reliever
Non-Proprietary Name:
Acetaminophen, Ibuprofen
Substance Name:
Acetaminophen; Ibuprofen
Usage Information:
•do not take more than directedAdults and children 12 years and over: take 2 caplets every 8 hours while symptoms persistChildren under 12 years: ask a doctor•do not take more than 6 caplets in 24 hours, unless directed by a doctor
11-Digit NDC Billing Format:
00363619923
NDC to RxNorm Crosswalk:
  • RxCUI: 2387532 - acetaminophen 250 MG / ibuprofen 125 MG Oral Tablet
  • RxCUI: 2387532 - APAP 250 MG / ibuprofen 125 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Walgreen Company
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETAMINOPHEN 250 mg/1
  • IBUPROFEN 125 mg/1
    • Pharmacologic Class(es):
  • Anti-Inflammatory Agents, Non-Steroidal - [CS]
  • Cyclooxygenase Inhibitors - [MoA] (Mechanism of Action)
  • Nonsteroidal Anti-inflammatory Drug - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA214836
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-16-2024
    Listing Expiration Date:
    12-31-2025
    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 0363-6199-23?

    The NDC Packaged Code 0363-6199-23 is assigned to a package of 1 bottle in 1 carton / 72 tablet, film coated in 1 bottle of Dual Back Pain Reliever, a human over the counter drug labeled by Walgreen Company. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 0363-6199 included in the NDC Directory?

    Yes, Dual Back Pain Reliever with product code 0363-6199 is active and included in the NDC Directory. The product was first marketed by Walgreen Company on February 16, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0363-6199-23?

    The 11-digit format is 00363619923. 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 4-4-2 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
    4-4-20363-6199-235-4-200363-6199-23