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  5. NDC Package Code: 70154-204-30 Triprolidine Hydrochloride

NDC Package 70154-204-30 Triprolidine Hydrochloride

Liquid 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:
70154-204-30
Package Description:
30 mL in 1 BOTTLE
Product Code:
70154-204
Proprietary Name:
Triprolidine Hydrochloride
Non-Proprietary Name:
Triprolidine Hydrochloride
Substance Name:
Triprolidine Hydrochloride
Usage Information:
Do not exceed recommended dosage.■ use only with enclosed dropper ■ do not use enclosed dropper for any other drug product ■ mL= milliliter ■ Professional Labeling: Take under guidance of Health Professionals. AGEDOSEChilden 4 to under 6 years of age:1 dropperful (1.0 mL) every 4 to 6 hours, not to exceed 4 doses (4.0 mL) in 24 hours, or as directed by a Doctor.Children 2 to under 4 years of age⅔ dropperful (0.67 mL) every 4 to 6 hours, not to exceed 4 doses (2.67 mL) in 24 hours, or as directed by a Doctor.Infants 4 months to under 2 years of age⅓ dropperful (0.33 mL) every 4 to 6 hours, not to exceed 4 doses (1.33 mL) in 24 hours, or as directed by a Doctor.
11-Digit NDC Billing Format:
70154020430
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:
    Monarch Pcm, Llc
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • TRIPROLIDINE HYDROCHLORIDE .938 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    08-19-2019
    End Marketing Date:
    10-31-2024
    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 70154-204-30?

    The NDC Packaged Code 70154-204-30 is assigned to a package of 30 ml in 1 bottle of Triprolidine Hydrochloride, a human over the counter drug labeled by Monarch Pcm, Llc. The product's dosage form is liquid and is administered via oral form.

    Is NDC 70154-204 included in the NDC Directory?

    Yes, Triprolidine Hydrochloride with product code 70154-204 is active and included in the NDC Directory. The product was first marketed by Monarch Pcm, Llc on August 19, 2019.

    What is the 11-digit format for NDC 70154-204-30?

    The 11-digit format is 70154020430. 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
    5-3-270154-204-305-4-270154-0204-30