1. Home
  2. Labeler Index
  3. Johnson & Johnson Consumer Inc.
  4. 50580-436
  5. NDC Package Code: 50580-436-01 Sudafed Pe Head Congestion Plus Pain

NDC Package 50580-436-01 Sudafed Pe Head Congestion Plus Pain

Ibuprofen And Phenylephrine Hydrochloride 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:
50580-436-01
Package Description:
2 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
50580-436
Proprietary Name:
Sudafed Pe Head Congestion Plus Pain
Non-Proprietary Name:
Ibuprofen And Phenylephrine Hydrochloride
Substance Name:
Ibuprofen; Phenylephrine Hydrochloride
Usage Information:
Do not take more than directedadults and children 12 years of age and over:take 1 caplet every 4 hours while symptoms persistdo not use more than 6 caplets in any 24-hour period unless directed by a doctorchildren under 12 years of age: do not use because this product contains too much medication for children under this age
11-Digit NDC Billing Format:
50580043601
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
2 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1369775 - ibuprofen 200 MG / phenylephrine HCl 10 MG Oral Tablet
  • RxCUI: 1369775 - ibuprofen 200 MG / phenylephrine hydrochloride 10 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Johnson & Johnson Consumer Inc.
    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):
  • IBUPROFEN 200 mg/1
  • PHENYLEPHRINE HYDROCHLORIDE 10 mg/1
    • Pharmacologic Class(es):
  • Adrenergic alpha1-Agonists - [MoA] (Mechanism of Action)
  • Anti-Inflammatory Agents, Non-Steroidal - [CS]
  • Cyclooxygenase Inhibitors - [MoA] (Mechanism of Action)
  • Nonsteroidal Anti-inflammatory Drug - [EPC] (Established Pharmacologic Class)
  • alpha-1 Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA203200
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-17-2019
    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 50580-436-01?

    The NDC Packaged Code 50580-436-01 is assigned to a package of 2 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack of Sudafed Pe Head Congestion Plus Pain, a human over the counter drug labeled by Johnson & Johnson Consumer Inc.. The product's dosage form is tablet, film coated and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 2 billable units per package.

    Is NDC 50580-436 included in the NDC Directory?

    Yes, Sudafed Pe Head Congestion Plus Pain with product code 50580-436 is active and included in the NDC Directory. The product was first marketed by Johnson & Johnson Consumer Inc. on June 17, 2019 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 NDC billing unit for package 50580-436-01?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 2.

    What is the 11-digit format for NDC 50580-436-01?

    The 11-digit format is 50580043601. 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
    5-3-250580-436-015-4-250580-0436-01