NDC Package 70518-1132-0 Labetalol 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:

70518-1132-0

Package Description:

30 TABLET, FILM COATED in 1 BLISTER PACK

Product Code:

70518-1132

Proprietary Name:

Labetalol Hydrochloride

Usage Information:

Labetalol hydrochloride tablets, USP are indicated in the management of hypertension. Labetalol hydrochloride tablets USP may be used alone or in combination with other antihypertensive agents, especially thiazide and loop diuretics.

11-Digit NDC Billing Format:

70518113200

Labeler Name:

Remedyrepack Inc.

Sample Package:

FDA Application Number:

ANDA207743

Marketing Category:

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

Start Marketing Date:

04-24-2018

End Marketing Date:

01-19-2023

Listing Expiration Date:

01-19-2023

Exclude Flag:

Code Structure:

70518 - Remedyrepack Inc.
- 70518-1132 - Labetalol Hydrochloride
  - 70518-1132-0 - 30 TABLET, FILM COATED in 1 BLISTER PACK

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
70518-1132-1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
70518-1132-2	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70518-1132-0?

The NDC Packaged Code 70518-1132-0 is assigned to a package of 30 tablet, film coated in 1 blister pack of Labetalol Hydrochloride, labeled by Remedyrepack Inc.. The product's dosage form is and is administered via form.

Is NDC 70518-1132 included in the NDC Directory?

No, Labetalol Hydrochloride with product code 70518-1132 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Remedyrepack Inc. on April 24, 2018 and its listing in the NDC Directory is set to expire on January 19, 2023 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70518-1132-0?

The 11-digit format is 70518113200. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-4-1	70518-1132-0	5-4-2	70518-1132-00

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