Testozole

Manufacturer: Advanced Pharmaceutical Technology, Inc.
Effective date: 2022-05-27
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 22:00:25

Label at a glance#

ProductTestozole

Active ingredientTESTOSTERONE, ANASTROZOLE

Label structure6 sections

Storage and handling

Store t controlled room temperature

Label contents#

Full prescribing information#

Indication:

INDICATIONS & USAGE SECTION

Estrogen Receptor Positive Metastatic Breast Cancer

Usual Dosage:

DOSAGE & ADMINISTRATION SECTION

180mg Testosterone & 12mg of Anastrozole

CAUTION:

SPL UNCLASSIFIED SECTION

Federal Law prohibits dispensing without prescription.

Storage:

STORAGE AND HANDLING SECTION

Store t controlled room temperature

Manufactured by:

SPL UNCLASSIFIED SECTION

ADVANCED PHARMACEUTICAL TECHNOLOGY

Phone: (914)358-5260

Elmsford, NY 10523

Testozole (57377-060-01)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Testozole

SPL UNCLASSIFIED SECTION

Testozole

HOW SUPPLIED SECTION

3 Sterile Pellets

DOSAGE FORMS & STRENGTHS SECTION

For subcutaneous implantation

Each pellet contains:

60mg Testosterone

4mg Anastrozole

Caution:

SAFE HANDLING WARNING SECTION

Federal Law prohibits dispensing without presciption.

STORAGE AND HANDLING SECTION

Store at controlled room temperature.

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

Testozole
Testosterone,USP
POVIDONE
STEARIC ACID
TESTOSTERONE
ANASTROZOLE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
57377-060	57377-060-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
POVIDONE	FZ989GH94E	IACT
STEARIC ACID	4ELV7Z65AP	IACT
TESTOSTERONE	3XMK78S47O	ACTIB
ANASTROZOLE	2Z07MYW1AZ	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2377d73f-84c0-e910-e063-6394a90a479c			d3c42530-07dd-8a7d-e053-2a95a90ab2b6	2024-10-02		Exact identifier spl set id: d3c42530-07dd-8a7d-e053-2a95a90ab2b6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.