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  5. NDC Package Code: 51990-201-06 Sorafenib

NDC Package 51990-201-06 Sorafenib

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
51990-201-06
Package Description:
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
51990-201
Proprietary Name:
Sorafenib
Non-Proprietary Name:
Sorafenib
Substance Name:
Sorafenib
Usage Information:
Sorafenib tablets are contraindicated in patients with known severe hypersensitivity to sorafenib or any other component of Sorafenib tablets.Sorafenib tablets in combination with carboplatin and paclitaxel are contraindicated in patients with squamous cell lung cancer [see Warnings and Precautions (5.8)]. Sorafenib tablets are contraindicated in patients with known severe hypersensitivity to sorafenib or any other component of Sorafenib tablets.Sorafenib tablets in combination with carboplatin and paclitaxel are contraindicated in patients with squamous cell lung cancer [see Warnings and Precautions (5.8)].
11-Digit NDC Billing Format:
51990020106
NDC to RxNorm Crosswalk:
  • RxCUI: 597747 - SORAfenib 200 MG Oral Tablet
  • RxCUI: 597747 - sorafenib 200 MG Oral Tablet
  • RxCUI: 597747 - sorafenib (as sorafenib tosylate) 200 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Yabao Pharmaceutical Co., Ltd. Beijing
    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):
  • SORAFENIB 200 mg/1
    • Pharmacologic Class(es):
  • Kinase Inhibitor - [EPC] (Established Pharmacologic Class)
  • Protein Kinase Inhibitors - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    ANDA209050
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-01-2022
    Listing Expiration 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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    51990-201-12120 TABLET, FILM COATED in 1 PACKAGE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51990-201-06?

    The NDC Packaged Code 51990-201-06 is assigned to a package of 60 tablet, film coated in 1 bottle, plastic of Sorafenib, a human prescription drug labeled by Yabao Pharmaceutical Co., Ltd. Beijing. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 51990-201 included in the NDC Directory?

    Yes, Sorafenib with product code 51990-201 is active and included in the NDC Directory. The product was first marketed by Yabao Pharmaceutical Co., Ltd. Beijing on December 01, 2022 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 51990-201-06?

    The 11-digit format is 51990020106. 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
    5-3-251990-201-065-4-251990-0201-06