NDC Package 64679-773-03 Ropinirole Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
64679-773-03
Package Description:
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Code:
Proprietary Name:
Ropinirole Hydrochloride
Usage Information:
Ropinirole Extended-release Tablets are indicated for the treatment of Parkinson's disease.
11-Digit NDC Billing Format:
64679077303
NDC to RxNorm Crosswalk:
  • RxCUI: 799054 - rOPINIRole 8 MG 24HR Extended Release Oral Tablet
  • RxCUI: 799054 - 24 HR ropinirole 8 MG Extended Release Oral Tablet
  • RxCUI: 799054 - ropinirole 8 MG (as ropinirole hydrochloride 9.12 MG) 24 HR Extended Release Oral Tablet
  • RxCUI: 799054 - ropinirole 8 MG 24 HR Extended Release Oral Tablet
  • RxCUI: 799055 - rOPINIRole 2 MG 24HR Extended Release Oral Tablet
  • Labeler Name:
    Wockhardt Usa Llc.
    Sample Package:
    No
    Start Marketing Date:
    08-15-2012
    Listing Expiration Date:
    12-31-2019
    Exclude Flag:
    I
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    64679-773-0130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    64679-773-0290 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    64679-773-0410 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
    64679-773-05100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 64679-773-03?

    The NDC Packaged Code 64679-773-03 is assigned to a package of 500 tablet, film coated, extended release in 1 bottle of Ropinirole Hydrochloride, labeled by Wockhardt Usa Llc.. The product's dosage form is and is administered via form.

    Is NDC 64679-773 included in the NDC Directory?

    No, Ropinirole Hydrochloride with product code 64679-773 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Wockhardt Usa Llc. on August 15, 2012 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 64679-773-03?

    The 11-digit format is 64679077303. 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
    5-3-264679-773-035-4-264679-0773-03