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  5. NDC Package Code: 70677-0079-1 Sunmark Fexofenadine Hydrochloride

NDC Package 70677-0079-1 Sunmark Fexofenadine Hydrochloride

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 discontinued by the firm.

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:
70677-0079-1
Package Description:
12 BLISTER PACK in 1 CARTON / 1 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
70677-0079
Proprietary Name:
Sunmark Fexofenadine Hydrochloride
Usage Information:
Adults and children 12 years of age and overtake one 60 mg tablet with water every 12 hours; do not take more than 2 tablets in 24 hourschildren under 12 years of agedo not useadults 65 years of age and olderask a doctorconsumers with kidney diseaseask a doctor
11-Digit NDC Billing Format:
70677007901
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
12 EA
Labeler Name:
Strategic Sourcing Services Llc
Sample Package:
No
FDA Application Number:
ANDA076447
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
08-21-2019
End Marketing Date:
08-31-2021
Listing Expiration Date:
08-31-2021
Exclude Flag:
D
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 70677-0079-1?

The NDC Packaged Code 70677-0079-1 is assigned to a package of 12 blister pack in 1 carton / 1 tablet, film coated in 1 blister pack of Sunmark Fexofenadine Hydrochloride, labeled by Strategic Sourcing Services Llc. The product's dosage form is and is administered via form.

Is NDC 70677-0079 included in the NDC Directory?

No, Sunmark Fexofenadine Hydrochloride with product code 70677-0079 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Strategic Sourcing Services Llc on August 21, 2019 and its listing in the NDC Directory is set to expire on August 31, 2021 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 70677-0079-1?

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 12.

What is the 11-digit format for NDC 70677-0079-1?

The 11-digit format is 70677007901. 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 5-4-1 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
5-4-170677-0079-15-4-270677-0079-01