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  5. NDC Package Code: 55758-313-18 Antigrip Nighttime

NDC Package 55758-313-18 Antigrip Nighttime

Acetaminophen,Chlorpheniramine Maleate,Dextromethorphan Hbr,Phenylephrine Hci Powder, For - 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:
55758-313-18
Package Description:
18 POUCH in 1 CARTON / 1 POWDER, FOR SOLUTION in 1 POUCH
Product Code:
55758-313
Proprietary Name:
Antigrip Nighttime
Non-Proprietary Name:
Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hbr, Phenylephrine Hci
Substance Name:
Acetaminophen; Chlorpheniramine Maleate; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride
Usage Information:
DO NOT EXCEED RECOMMENDED DOSE take every 4 hours; do not exceed 6 packets in a 24 hour period dissolve the contents of one packet into 8 oz. of hot water and sip while hot; consume entire drink within 10-15 minutesif using a microwave; add contents of one packet to 8 oz. of cool water, stir briskly before and after heating. Do not overheat.AgeDoseadults and children 12 years of age and overone packet every 4 hourschildren under 12 years of agedo not use; unless directed by a doctor children under 6 years of agedo not use
11-Digit NDC Billing Format:
55758031318
NDC to RxNorm Crosswalk:
  • RxCUI: 1534666 - acetaminophen 650 MG / chlorpheniramine maleate 4 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Powder for Oral Solution
  • RxCUI: 1534666 - acetaminophen 650 MG / chlorpheniramine maleate 4 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Powder for Oral Solution
  • RxCUI: 1534666 - acetaminophen 650 MG / chlorpheniramine maleate 4 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Packet for Oral Solution
  • RxCUI: 1534666 - acetaminophen 650 MG / chlorpheniramine maleate 4 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Granules for Oral Solution
  • RxCUI: 1534666 - APAP 650 MG / Chlorpheniramine Maleate 4 MG / Dextromethorphan Hydrobromide 20 MG / Phenylephrine Hydrochloride 10 MG Powder for Oral Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Pharmadel Llc
    Dosage Form:
    Powder, For Solution - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a solution.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETAMINOPHEN 650 mg/1
  • CHLORPHENIRAMINE MALEATE 4 mg/1
  • DEXTROMETHORPHAN HYDROBROMIDE 20 mg/1
  • PHENYLEPHRINE HYDROCHLORIDE 10 mg/1
    • Pharmacologic Class(es):
  • Adrenergic alpha1-Agonists - [MoA] (Mechanism of Action)
  • Histamine H1 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
  • Sigma-1 Agonist - [EPC] (Established Pharmacologic Class)
  • Sigma-1 Receptor Agonists - [MoA] (Mechanism of Action)
  • Uncompetitive N-methyl-D-aspartate Receptor Antagonist - [EPC] (Established Pharmacologic Class)
  • Uncompetitive NMDA Receptor Antagonists - [MoA] (Mechanism of Action)
  • alpha-1 Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
    • 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:
    03-28-2019
    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 55758-313-18?

    The NDC Packaged Code 55758-313-18 is assigned to a package of 18 pouch in 1 carton / 1 powder, for solution in 1 pouch of Antigrip Nighttime, a human over the counter drug labeled by Pharmadel Llc. The product's dosage form is powder, for solution and is administered via oral form.

    Is NDC 55758-313 included in the NDC Directory?

    Yes, Antigrip Nighttime with product code 55758-313 is active and included in the NDC Directory. The product was first marketed by Pharmadel Llc on March 28, 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 11-digit format for NDC 55758-313-18?

    The 11-digit format is 55758031318. 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
    5-3-255758-313-185-4-255758-0313-18