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  5. NDC Package Code: 55629-012-01 Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride

NDC Package 55629-012-01 Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
55629-012-01
Package Description:
48 POUCH in 1 CARTON / 300 CAPSULE, LIQUID FILLED in 1 POUCH (55629-012-02)
Product Code:
55629-012
Proprietary Name:
Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Usage Information:
Take only as recommended - see OVERDOSE warningdo not exceed 6 doses per 24 hoursAdults and children 12 years of age and older2 LiquiCaps with water every 4 hoursChildren under 12 years of ageask doctorWhen using other DayQuil or NyQuil products, carefully read each label to insure correct dosing
11-Digit NDC Billing Format:
55629001201
NDC to RxNorm Crosswalk:
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
Labeler Name:
One2zee Limited Liability Company
Sample Package:
No
FDA Application Number:
part341
Marketing Category:
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date:
03-01-2021
Listing Expiration Date:
12-31-2024
Exclude Flag:
I
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 55629-012-01?

The NDC Packaged Code 55629-012-01 is assigned to a package of 48 pouch in 1 carton / 300 capsule, liquid filled in 1 pouch (55629-012-02) of Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, labeled by One2zee Limited Liability Company. The product's dosage form is and is administered via form.

Is NDC 55629-012 included in the NDC Directory?

No, Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride with product code 55629-012 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by One2zee Limited Liability Company on March 01, 2021 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 55629-012-01?

The 11-digit format is 55629001201. 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
5-3-255629-012-015-4-255629-0012-01