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  5. NDC Package Code: 10702-150-16 Hydrocodone Bitartrate And Homatropine Methylbromide

NDC Package 10702-150-16 Hydrocodone Bitartrate And Homatropine Methylbromide

Hydrocodone Bitartrate And Homatropine Methylbromide Oral Solution 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:
10702-150-16
Package Description:
473 mL in 1 BOTTLE
Product Code:
10702-150
Proprietary Name:
Hydrocodone Bitartrate And Homatropine Methylbromide
Non-Proprietary Name:
Hydrocodone Bitartrate And Homatropine Methylbromide Oral Solution
Substance Name:
Homatropine Methylbromide; Hydrocodone Bitartrate
Usage Information:
Hydrocodone bitartrate and homatropine methylbromide is indicated for the symptomatic relief of cough in adults and children 6 years of age and older.
11-Digit NDC Billing Format:
10702015016
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
473 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 992668 - HYDROcodone bitartrate 5 MG / homatropine methylbromide 1.5 MG in 5 mL Oral Solution
  • RxCUI: 992668 - homatropine methylbromide 0.3 MG/ML / hydrocodone bitartrate 1 MG/ML Oral Solution
  • RxCUI: 992668 - homatropine methylbromide 1.5 MG / hydrocodone bitartrate 5 MG per 5 ML Syrup
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Kvk-tech, Inc.
    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):
  • HOMATROPINE METHYLBROMIDE 1.5 mg/5mL
  • HYDROCODONE BITARTRATE 5 mg/5mL
    • Pharmacologic Class(es):
  • Opioid Agonist - [EPC] (Established Pharmacologic Class)
  • Opioid Agonists - [MoA] (Mechanism of Action)
    • DEA Schedule:
    Schedule II (CII) Substances
    Sample Package:
    No
    FDA Application Number:
    ANDA207487
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-21-2017
    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 10702-150-16?

    The NDC Packaged Code 10702-150-16 is assigned to a package of 473 ml in 1 bottle of Hydrocodone Bitartrate And Homatropine Methylbromide, a human prescription drug labeled by Kvk-tech, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 10702-150 included in the NDC Directory?

    Yes, Hydrocodone Bitartrate And Homatropine Methylbromide with product code 10702-150 is active and included in the NDC Directory. The product was first marketed by Kvk-tech, Inc. on February 21, 2017 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 10702-150-16?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 473.

    What is the 11-digit format for NDC 10702-150-16?

    The 11-digit format is 10702015016. 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
    5-3-210702-150-165-4-210702-0150-16