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  5. NDC Package Code: 70868-740-16 Miclara Dm

NDC Package 70868-740-16 Miclara Dm

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
70868-740-16
Package Description:
473 mL in 1 BOTTLE
Product Code:
70868-740
Proprietary Name:
Miclara Dm
Usage Information:
Do not exceed recommended dosage.AgeDoseAdults and children 12 years of age and older:1 teaspoonful (5mL) every 4 hours, not to exceed 4 teaspoonfuls (20mL) in a 24-hour period or as directed by a doctorChildren 6 to under 12 years of age:½ teaspoonful (2.5mL) every 4 hours, not to exceed 2 teaspoonfuls (10mL) in a 24-hour period or as directed by a doctorChildren under 6 years of age:Consult a doctor
11-Digit NDC Billing Format:
70868074016
NDC to RxNorm Crosswalk:
  • RxCUI: 1492052 - dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG / triprolidine HCl 2.5 MG in 5 mL Oral Solution
  • RxCUI: 1492052 - dextromethorphan hydrobromide 4 MG/ML / phenylephrine hydrochloride 2 MG/ML / triprolidine hydrochloride 0.5 MG/ML Oral Solution
  • RxCUI: 1492052 - dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG / triprolidine hydrochloride 2.5 MG per 5 ML Oral Solution
    • Labeler Name:
    Key Therapeutics
    Sample Package:
    No
    Start Marketing Date:
    09-01-2020
    Listing Expiration Date:
    12-31-2023
    Exclude Flag:
    I
    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 70868-740-16?

    The NDC Packaged Code 70868-740-16 is assigned to a package of 473 ml in 1 bottle of Miclara Dm, labeled by Key Therapeutics. The product's dosage form is and is administered via form.

    Is NDC 70868-740 included in the NDC Directory?

    No, Miclara Dm with product code 70868-740 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Key Therapeutics on September 01, 2020 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70868-740-16?

    The 11-digit format is 70868074016. 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
    5-3-270868-740-165-4-270868-0740-16