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  5. NDC Package Code: 57377-060-01 Testozole

NDC Package 57377-060-01 Testozole

Testosterone, Usp Pellet, Implantable Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
57377-060-01
Package Description:
3 PELLET, IMPLANTABLE in 1 AMPULE
Product Code:
57377-060
Proprietary Name:
Testozole
Non-Proprietary Name:
Testosterone, Usp
Substance Name:
Anastrozole; Testosterone
11-Digit NDC Billing Format:
57377006001
Product Type:
Human Prescription Drug
Labeler Name:
Advanced Pharmaceutical Technology, Inc.
Dosage Form:
Pellet, Implantable - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding; they are intended for implantation in the body (usually subcutaneously) for the purpose of providing continuous release of the drug over long periods of time.
Administration Route(s):
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
    • Active Ingredient(s):
  • ANASTROZOLE 4 mg/1
  • TESTOSTERONE 60 mg/1
    • Pharmacologic Class(es):
  • Androgen Receptor Agonists - [MoA] (Mechanism of Action)
  • Androgen - [EPC] (Established Pharmacologic Class)
  • Androstanes - [CS]
  • Aromatase Inhibitor - [EPC] (Established Pharmacologic Class)
  • Aromatase Inhibitors - [MoA] (Mechanism of Action)
    • DEA Schedule:
    Schedule III (CIII) Substances
    Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    01-01-2021
    Listing Expiration Date:
    12-31-2024
    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 57377-060-01?

    The NDC Packaged Code 57377-060-01 is assigned to a package of 3 pellet, implantable in 1 ampule of Testozole, a human prescription drug labeled by Advanced Pharmaceutical Technology, Inc.. The product's dosage form is pellet, implantable and is administered via subcutaneous form.

    Is NDC 57377-060 included in the NDC Directory?

    Yes, Testozole with product code 57377-060 is active and included in the NDC Directory. The product was first marketed by Advanced Pharmaceutical Technology, Inc. on January 01, 2021 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 57377-060-01?

    The 11-digit format is 57377006001. 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
    5-3-257377-060-015-4-257377-0060-01