NDC Compounded Drug 73271-1155-1 Triamcinolone Acetonide; Testosterone

Pellet Subcutaneous

Table of Contents

    1. Compounded Product Information
    2. NDC Crossover Products Matching Testosterone/triamcinolone 55 Mg/ 0.011 Mg Research And Development/experimental/not For Distribution
    3. Frequently Asked Questions

Compounded Drug Product Information

NDC Product Code 73271-1155
NDC Package Code 73271-1155-1
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.		 73271115501
Package Description 1 PELLET in 1 VIAL
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.		 Testosterone/triamcinolone 55 Mg/ 0.011 Mg Research And Development/experimental/not For Distribution
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/triamcinolone 55 Mg/ 0.011 Mg Research And Development/experimental/not For Distribution
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.		 Triamcinolone Acetonide; Testosterone
Dosage Form Pellet - 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.
Route Name Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
Marketing Category OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Code 73271
Labeler Name What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		 Right Value Drug Stores Llc Dba Carie Boyd's Prescription Shop
Substance Name Triamcinolone Acetonide; Testosterone
Active Ingredients Information .011 mg; 55 mg
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 2022-2

NDC Crossover Products Matching Triamcinolone Acetonide; Testosterone

NDC crossover of Testosterone/triamcinolone 55 Mg/ 0.011 Mg Research And Development/experimental/not For Distribution with NDC 73271-1155 a human compounded drug with other similar products matching the same substance name (Triamcinolone Acetonide; Testosterone) and the same administration route (subcutaneous) or dosage form (pellet).

Frequently Asked Questions

What is the NDC number assigned to Testosterone/triamcinolone 200 Mg/ 0.04 Mg Research And Development/experimental/not For Distribution?

Testosterone/triamcinolone 200 Mg/ 0.04 Mg Research And Development/experimental/not For Distribution was assigned by its manufacturer with NDC product code 73271-1155. 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/triamcinolone 200 Mg/ 0.04 Mg Research And Development/experimental/not For Distribution?

The NDC package code 73271-1155-1 was assigned to a 1 PELLET in 1 VIAL of triamcinolone acetonide; testosterone administered subcutaneous via pellet.

Who manufactures this product?

Testosterone/triamcinolone 200 Mg/ 0.04 Mg Research And Development/experimental/not For Distribution is manufactured by an outsourced facility and labeled by Right Value Drug Stores Llc Dba Carie Boyd's Prescription Shop. 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 2 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by Right Value Drug Stores llc dba Carie Boyd's Prescription Shop with NDC product codes 73271-1112-1 and 73271-1120-1.