NDC Package 58552-333-20 Giltuss D Allergy And Congestion

Chlorpheniramine Maleate,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:
58552-333-20
Package Description:
10 POUCH in 1 BOX / 2 TABLET in 1 POUCH
Product Code:
Proprietary Name:
Giltuss D Allergy And Congestion
Non-Proprietary Name:
Chlorpheniramine Maleate, Phenylephrine Hcl
Substance Name:
Chlorpheniramine Maleate; Phenylephrine Hydrochloride
Usage Information:
Uses Temporarily relieves these symptoms due to hay fever (allergic rhinitis) or other upper respiratory allergies: runny nosesneezingitchy, watery eyesnasal congestionitching of the nose or throatsinus congestion and pressure
11-Digit NDC Billing Format:
58552033320
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
10 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1367227 - chlorpheniramine maleate 3.5 MG / phenylephrine HCl 10 MG Oral Tablet
  • RxCUI: 1367227 - chlorpheniramine maleate 3.5 MG / phenylephrine hydrochloride 10 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Gil Pharmaceutical Corp
    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:
    11-17-2016
    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 58552-333-20?

    The NDC Packaged Code 58552-333-20 is assigned to a package of 10 pouch in 1 box / 2 tablet in 1 pouch of Giltuss D Allergy And Congestion, a human over the counter drug labeled by Gil Pharmaceutical Corp. The product's dosage form is tablet and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 10 billable units per package.

    Is NDC 58552-333 included in the NDC Directory?

    Yes, Giltuss D Allergy And Congestion with product code 58552-333 is active and included in the NDC Directory. The product was first marketed by Gil Pharmaceutical Corp on November 17, 2016 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 58552-333-20?

    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 10.

    What is the 11-digit format for NDC 58552-333-20?

    The 11-digit format is 58552033320. 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
    5-3-258552-333-205-4-258552-0333-20