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  5. NDC Package Code: 68382-602-07 Clonidine Hydrochloride

NDC Package 68382-602-07 Clonidine 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:
68382-602-07
Package Description:
1 VIAL in 1 CARTON / 10 mL in 1 VIAL
Product Code:
68382-602
Proprietary Name:
Clonidine Hydrochloride
Usage Information:
Clonidine hydrochloride injection is indicated in combination with opiates for the treatment of severe pain in cancer patients that is not adequately relieved by opioid analgesics alone. Epidural clonidine is more likely to be effective in patients with neuropathic pain than somatic or visceral pain (see Clinical Trials). The safety of this drug product has only been established in a highly selected group of cancer patients, and only after an adequate trial of opioid analgesia. Other use is of unproven safety and is not recommended. In a rare patient, the potential benefits may outweigh the known risks (see WARNINGS).
11-Digit NDC Billing Format:
68382060207
Labeler Name:
Zydus Pharmaceuticals Usa Inc.
Sample Package:
No
FDA Application Number:
ANDA202601
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
01-31-2018
End Marketing Date:
05-31-2025
Listing Expiration Date:
05-31-2025
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 68382-602-07?

The NDC Packaged Code 68382-602-07 is assigned to a package of 1 vial in 1 carton / 10 ml in 1 vial of Clonidine Hydrochloride, labeled by Zydus Pharmaceuticals Usa Inc.. The product's dosage form is and is administered via form.

Is NDC 68382-602 included in the NDC Directory?

No, Clonidine Hydrochloride with product code 68382-602 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Zydus Pharmaceuticals Usa Inc. on January 31, 2018 and its listing in the NDC Directory is set to expire on May 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 68382-602-07?

The 11-digit format is 68382060207. 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
5-3-268382-602-075-4-268382-0602-07