NDC Package 69660-201-91 Rubraca

Rucaparib Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
69660-201-91
Package Description:
60 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Rubraca
Non-Proprietary Name:
Rucaparib
Substance Name:
Rucaparib Camsylate
Usage Information:
This medication is used to treat certain cancers (such as ovarian, fallopian tube, peritoneal, prostate cancer). It works by slowing or stopping the growth of cancer cells.
11-Digit NDC Billing Format:
69660020191
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
60 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1862584 - rucaparib 300 MG Oral Tablet
  • RxCUI: 1862584 - rucaparib (as rucaparib camsylate) 300 MG Oral Tablet
  • RxCUI: 1862590 - Rubraca 300 MG Oral Tablet
  • RxCUI: 1862590 - rucaparib 300 MG Oral Tablet [Rubraca]
  • RxCUI: 1862590 - Rubraca (as rucaparib camisylate) 300 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Clovis Oncology, Inc.
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA209115
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    12-19-2016
    End Marketing Date:
    12-31-2025
    Exclude Flag:
    N
    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 69660-201-91?

    The NDC Packaged Code 69660-201-91 is assigned to a package of 60 tablet, film coated in 1 bottle of Rubraca, a human prescription drug labeled by Clovis Oncology, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 60 billable units per package.

    Is NDC 69660-201 included in the NDC Directory?

    Yes, Rubraca with product code 69660-201 is active and included in the NDC Directory. The product was first marketed by Clovis Oncology, Inc. on December 19, 2016.

    What is the NDC billing unit for package 69660-201-91?

    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 60.

    What is the 11-digit format for NDC 69660-201-91?

    The 11-digit format is 69660020191. 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
    5-3-269660-201-915-4-269660-0201-91