NDC Package 68682-212-10 Trientine Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Package Information
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:

68682-212-10

Package Description:

1 BOTTLE in 1 CARTON / 100 CAPSULE in 1 BOTTLE

Product Code:

68682-212

Proprietary Name:

Trientine Hydrochloride

Usage Information:

Trientine Hydrochloride Capsules are indicated in the treatment of patients with Wilson's disease who are intolerant of penicillamine. Clinical experience with Trientine Hydrochloride Capsules is limited and alternate dosing regimens have not been well-characterized; all endpoints in determining an individual patient's dose have not been well defined. Trientine Hydrochloride Capsules and penicillamine cannot be considered interchangeable. Trientine Hydrochloride Capsules should be used when continued treatment with penicillamine is no longer possible because of intolerable or life endangering side effects.Unlike penicillamine, Trientine Hydrochloride Capsules are not recommended in cystinuria or rheumatoid arthritis. The absence of a sulfhydryl moiety renders it incapable of binding cystine and, therefore, it is of no use in cystinuria. In 15 patients with rheumatoid arthritis, Trientine Hydrochloride Capsules were reported not to be effective in improving any clinical or biochemical parameter after 12 weeks of treatment.Trientine Hydrochloride Capsules are not indicated for treatment of biliary cirrhosis.

11-Digit NDC Billing Format:

68682021210

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

1 EA

Labeler Name:

Oceanside Pharmaceutials

Sample Package:

FDA Application Number:

NDA019194

Marketing Category:

NDA AUTHORIZED GENERIC - A product marketed as a "generic" drug under an approved New Drug Application (NDA), rather than an Abbreviated New Drug Application (ANDA),.

Start Marketing Date:

02-09-2018

End Marketing Date:

04-30-2024

Listing Expiration Date:

04-30-2024

Exclude Flag:

Code Structure:

68682 - Oceanside Pharmaceutials
- 68682-212 - Trientine Hydrochloride
  - 68682-212-10 - 1 BOTTLE in 1 CARTON / 100 CAPSULE 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.

Frequently Asked Questions

What is NDC 68682-212-10?

The NDC Packaged Code 68682-212-10 is assigned to a package of 1 bottle in 1 carton / 100 capsule in 1 bottle of Trientine Hydrochloride, labeled by Oceanside Pharmaceutials. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

Is NDC 68682-212 included in the NDC Directory?

No, Trientine Hydrochloride with product code 68682-212 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Oceanside Pharmaceutials on February 09, 2018 and its listing in the NDC Directory is set to expire on April 30, 2024 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 68682-212-10?

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 1.

What is the 11-digit format for NDC 68682-212-10?

The 11-digit format is 68682021210. 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	68682-212-10	5-4-2	68682-0212-10

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