NDC Package 70985-002-04 Cetirizine Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Package Information
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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:

70985-002-04

Package Description:

90 TABLET in 1 BOTTLE

Product Code:

70985-002

Proprietary Name:

Cetirizine Hydrochloride

Usage Information:

Adults and children 6 years and overone 10 mg tablet once daily, do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less sever symptoms.Adults 65 years and overAsk a doctorChildren under 6 years of ageAsk a doctorConsumers with liver or kidney diseaseAsk a doctor

11-Digit NDC Billing Format:

70985000204

NDC to RxNorm Crosswalk:

RxCUI: 1014678 - cetirizine HCl 10 MG Oral Tablet
RxCUI: 1014678 - cetirizine hydrochloride 10 MG Oral Tablet

Labeler Name:

Drug Ocean Llc

Sample Package:

FDA Application Number:

ANDA077829

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

11-08-2016

End Marketing Date:

11-01-2025

Listing Expiration Date:

11-01-2025

Exclude Flag:

Code Structure:

70985 - Drug Ocean Llc
- 70985-002 - Cetirizine Hydrochloride
  - 70985-002-04 - 90 TABLET in 1 BOTTLE

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.

Other Product Packages

The following packages are also available for this product:

NDC Package Code	Package Description
70985-002-01	100 TABLET in 1 BOTTLE
70985-002-02	500 TABLET in 1 BOTTLE
70985-002-03	30 TABLET in 1 BOTTLE
70985-002-05	300 TABLET in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70985-002-04?

The NDC Packaged Code 70985-002-04 is assigned to a package of 90 tablet in 1 bottle of Cetirizine Hydrochloride, labeled by Drug Ocean Llc. The product's dosage form is and is administered via form.

Is NDC 70985-002 included in the NDC Directory?

No, Cetirizine Hydrochloride with product code 70985-002 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Drug Ocean Llc on November 08, 2016 and its listing in the NDC Directory is set to expire on November 01, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70985-002-04?

The 11-digit format is 70985000204. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	70985-002-04	5-4-2	70985-0002-04

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