NDC Compounded Drug 26436-5551-1 Estriol; Testosterone; Estradiol; Progesterone

Gel Topical

Compounded Drug Product Information

NDC Product Code 26436-5551
NDC Package Code 26436-5551-1
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.
Package Description 20 g in 1 BOTTLE, PUMP
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.
Biest 2mg Progesterone 100mg Testosterone 0.5mg/gm
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.
Biest 2mg Progesterone 100mg Testosterone 0.5mg/gm
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.
Estriol; Testosterone; Estradiol; Progesterone
Dosage Form Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Route Name Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Labeler Code 26436
Labeler Name What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Hybrid Pharma
Substance Name Estriol; Testosterone; Estradiol; Progesterone
Active Ingredients Information 1.6 mg/1 g; .5 mg/1 g; .4 mg/1 g; 100 mg/1 g
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 2021-2

Frequently Asked Questions

What is the NDC number assigned to Biest 2mg Progesterone 100mg Testosterone 0.5mg/gm?

Biest 2mg Progesterone 100mg Testosterone 0.5mg/gm was assigned by its manufacturer with NDC product code 26436-5551. 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 Biest 2mg Progesterone 100mg Testosterone 0.5mg/gm?

The NDC package code 26436-5551-1 was assigned to a 20 g in 1 BOTTLE, PUMP of estriol; testosterone; estradiol; progesterone administered topical via gel.

Who manufactures this product?

Biest 2mg Progesterone 100mg Testosterone 0.5mg/gm is manufactured by an outsourced facility and labeled by Hybrid Pharma. 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.