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  5. NDC Package Code: 55758-501-72 Antigrip Flu

NDC Package 55758-501-72 Antigrip Flu

Acetaminophen,Dextromethorphan Hbr,Phenylephrine Hcl Tablet, Effervescent 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:
55758-501-72
Package Description:
36 POUCH in 1 CARTON / 2 TABLET, EFFERVESCENT in 1 POUCH
Product Code:
55758-501
Proprietary Name:
Antigrip Flu
Non-Proprietary Name:
Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride
Usage Information:
■ adults and children 12 years of age and older: take two (2) tablets fully dissolved in a 4 oz glass of water every 4 hours. Do not exceed 12 tablets in 24 hours or as directed by a doctor. ■ children under 12 years of age: do not use
11-Digit NDC Billing Format:
55758050172
NDC to RxNorm Crosswalk:
  • RxCUI: 2691101 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Effervescent Oral Tablet
  • RxCUI: 2691101 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Effervescent Oral Tablet
  • RxCUI: 2691101 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Effervescent Oral Tablet
Product Type:
Human Otc Drug
Labeler Name:
Pharmadel Llc
Dosage Form:
Tablet, Effervescent - A solid dosage form containing mixtures of acids (e.g., citric acid, tartaric acid) and sodium bicarbonate, which release carbon dioxide when dissolved in water; it is intended to be dissolved or dispersed in water before administration.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
11-01-2024
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 55758-501-72?

The NDC Packaged Code 55758-501-72 is assigned to a package of 36 pouch in 1 carton / 2 tablet, effervescent in 1 pouch of Antigrip Flu, a human over the counter drug labeled by Pharmadel Llc. The product's dosage form is tablet, effervescent and is administered via oral form.

Is NDC 55758-501 included in the NDC Directory?

Yes, Antigrip Flu with product code 55758-501 is active and included in the NDC Directory. The product was first marketed by Pharmadel Llc on November 01, 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 55758-501-72?

The 11-digit format is 55758050172. 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
5-3-255758-501-725-4-255758-0501-72