NDC Package 0536-1289-35 Sinus Congestion And Pain Maximum Strength

Acetaminophen,Phenylephrine Hcl Tablet 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:
0536-1289-35
Package Description:
2 BLISTER PACK in 1 CARTON / 12 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Sinus Congestion And Pain Maximum Strength
Non-Proprietary Name:
Acetaminophen, Phenylephrine Hcl
Substance Name:
Acetaminophen; Phenylephrine Hydrochloride
Usage Information:
Do not use more than directed adults and children 12 years and overtake 2 caplets every 4 hoursdo not take more than 10 caplets in 24 hourschildren under 12 years: ask a doctor
11-Digit NDC Billing Format:
00536128935
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: 1046378 - acetaminophen 325 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1046378 - acetaminophen 325 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1046378 - APAP 325 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Rugby Laboratories
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    05-21-2020
    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 0536-1289-35?

    The NDC Packaged Code 0536-1289-35 is assigned to a package of 2 blister pack in 1 carton / 12 tablet in 1 blister pack of Sinus Congestion And Pain Maximum Strength, a human over the counter drug labeled by Rugby Laboratories. The product's dosage form is tablet and is administered via oral form.

    Is NDC 0536-1289 included in the NDC Directory?

    Yes, Sinus Congestion And Pain Maximum Strength with product code 0536-1289 is active and included in the NDC Directory. The product was first marketed by Rugby Laboratories on May 21, 2020 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 NDC billing unit for package 0536-1289-35?

    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 0536-1289-35?

    The 11-digit format is 00536128935. 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
    4-4-20536-1289-355-4-200536-1289-35