NDC Package 28595-801-30 Histex Pd Drops

Triprolidine Hydrochloride Syrup 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:
28595-801-30
Package Description:
1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Histex Pd Drops
Non-Proprietary Name:
Triprolidine Hydrochloride
Substance Name:
Triprolidine Hydrochloride
Usage Information:
Do not exceed recommended dosage.For dosing, use only the enclosed dropper and not with any other drug product.AGEDOSEAdults & Children 12 years of age or older:2.67 mL (2.5 milligrams) every 4 to 6 hours, not to exceed 10.67 mL (10 milligrams in 24 hours, or as directed by a doctor.Children 6 to under 12 years of age: 1.33 mL (1.25 milligrams) every 4 to 6 hours, not to exceed 5.33 mL (5 milligrams in 24 hours, or as directed by a doctor.Children under 6 years of age:Consult a doctor.
11-Digit NDC Billing Format:
28595080130
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1491649 - triprolidine HCl 0.938 MG in 1 mL Oral Solution
  • RxCUI: 1491649 - triprolidine hydrochloride 0.938 MG/ML Oral Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Allegis Pharmaceuticals, Llc
    Dosage Form:
    Syrup - An oral solution containing high concentrations of sucrose or other sugars; the term has also been used to include any other liquid dosage form prepared in a sweet and viscid vehicle, including oral suspensions.
    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:
    03-06-2014
    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 28595-801-30?

    The NDC Packaged Code 28595-801-30 is assigned to a package of 1 bottle in 1 carton / 30 ml in 1 bottle of Histex Pd Drops, a human over the counter drug labeled by Allegis Pharmaceuticals, Llc. The product's dosage form is syrup and is administered via oral form.

    Is NDC 28595-801 included in the NDC Directory?

    Yes, Histex Pd Drops with product code 28595-801 is active and included in the NDC Directory. The product was first marketed by Allegis Pharmaceuticals, Llc on March 06, 2014 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 28595-801-30?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 28595-801-30?

    The 11-digit format is 28595080130. 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
    5-3-228595-801-305-4-228595-0801-30