NDC Compounded Drug 57377-200-00 Testosterone Cypionate

Injection Intramuscular

Table of Contents

    1. Compounded Product Information
    2. NDC Crossover Products Matching Testo-200
    3. Frequently Asked Questions

Compounded Drug Product Information

NDC Product Code 57377-200
NDC Package Code 57377-200-00
11-Digit NDC Billing Format NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.		 57377020000
Package Description 10 mL in 1 VIAL, MULTI-DOSE
Product Type What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.		 Human Compounded Drug
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.		 Testo-200
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.		 Testosterone Cypionate Inj.
Substance Name What is the Substance Name?
An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.		 Testosterone Cypionate
Usage Information Product Usage Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.		 This medication is used in men who do not make enough of a natural substance called testosterone. In males, testosterone is responsible for many normal functions, including growth and development of the genitals, muscles, and bones. It also helps cause normal sexual development (puberty) in boys. Testosterone belongs to a class of drugs known as androgens. It works by affecting many body systems so that the body can develop and function normally. Testosterone may also be used in certain adolescent boys to cause puberty in those with delayed puberty. It may also be used to treat certain types of breast cancer in women.
Dosage Form Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Route Name Intramuscular - Administration within a muscle.
Marketing Category OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Code 57377
Labeler Name What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		 Advanced Pharmaceutical Technology, Inc.
Substance Name Testosterone Cypionate
Active Ingredients Information 200 mg/1 mL
DEA Schedule What is the Drug Enforcement Administration (DEA) CIII Schedule?
The controlled substances in the CIII schedule have an abuse potential and dependence liability less than those in schedules CI and CII, and have an accepted medical use in the United States. Schedule CIII controlled substances include preparations containing limited quantities of certain narcotic drugs, and other nonnarcotic drugs such as: derivatives of barbituric acid, except those that are listed in another schedule, glutethimide (Doriden), methyprylon (Noludar), nalorphine, benzphetamine, chlorphentermine, clortermine, and phendimetrazine.		 Schedule III (CIII) Substances
Reporting Period 2024-2

NDC Crossover Products Matching Testosterone Cypionate

NDC crossover of Testo-200 with NDC 57377-200 a human compounded drug with other similar products matching the same substance name (Testosterone Cypionate) and the same administration route (intramuscular) or dosage form (injection).

Frequently Asked Questions

What is the NDC number assigned to Testosterone Cypionate 200 Mg/ml Miglyol 812n 30ml Ndc 73271-1226-2?

Testosterone Cypionate 200 Mg/ml Miglyol 812n 30ml Ndc 73271-1226-2 was assigned by its manufacturer with NDC product code 57377-200. This product is a drug classified as a human compounded drug. Compounded drugs are medications created by combining or altering existing drugs to meet the specific needs of certain patients. The NDC directory only includes information about compounded drugs from facilities that choose to assign NDC numbers to their products.

Which are the NDC package codes for Testosterone Cypionate 200 Mg/ml Miglyol 812n 30ml Ndc 73271-1226-2?

The NDC package code 57377-200-00 was assigned to a 10 mL in 1 VIAL, MULTI-DOSE of testosterone cypionate administered intramuscular via injection.

Who manufactures this product?

Testosterone Cypionate 200 Mg/ml Miglyol 812n 30ml Ndc 73271-1226-2 is manufactured by an outsourced facility and labeled by Advanced Pharmaceutical Technology, Inc.. All compounded drugs included in the NDC directory are classified as "Outsourcing Facility Compounded Human Drug Product (Exempt from Approval Requirements)". Outsourcing facilities are a type of drug compounding facility regulated under Section 503B of the FD&C Act could be eligible for exemptions from drug registration if they meet all the conditions specified under Section 503B.

Which are the NDC crossover matchings for this product?

We found 22 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by Hybrid Pharma, Empower Pharmacy, AnazaoHealth Corporation and Right Value Drug Stores llc dba Carie Boyd Pharmaceuticals with NDC product codes 26436-5146-5, 26436-5600-5, 26436-5600-5, 26436-5600-5, 26436-5600-5, 72627-2100-1, 72682-8320-1, 72682-8320-1, 72682-8320-1, 72682-8320-1, 72682-8742-1, 72682-8742-1, 72682-9176-1, 72682-9176-1, 72682-9176-1, 72682-9176-1, 73271-1225-1, 73271-1225-1, 73271-1225-1, 73271-1226-2, 73271-1226-2 and 73271-1226-2.