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  4. NDC Product Code: 82797-130 Androtone Syrup

NDC 82797-130 Androtone Syrup

Tribulus Terr,Avena Sativa, Sterculia Acum,Nuphar Lut,Sabal Serr,Agnus Cast,Lycopodium - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 82797-130?
  5. Androtone Syrup Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes
  9. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 82797-130 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
82797-130
Proprietary Name:
Androtone Syrup
Non-Proprietary Name: [1]
Tribulus Terr, Avena Sativa, Sterculia Acum, Nuphar Lut, Sabal Serr, Agnus Cast, Lycopodium Clav, Gentiana Lut, Yohimbinum, Lecithin, Natrum Phos, Kali Phos, Calcarea Phos, Natrum Mur, Strychninum Sulph, Acidum Phos, Choloformum
Substance Name: [2]
Avena Sativa Whole; Calcium Phosphate; Cola Acuminata Whole; Gentiana Lutea Whole; Lecithin, Soybean; Lycopodium Clavatum Whole; Monobasic Potassium Phosphate; Nuphar Lutea Whole; Phosphoric Acid; Sabal Palmetto Whole; Sodium Chloride; Sodium Phosphate; Strychnine; Tribulus Terrestris Whole; Vitex Agnus-castus Whole; Yohimbine
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Syrup - An oral solution containing high concentrations of sucrose or other sugars; the term has also been used to include any other liquid dosage form prepared in a sweet and viscid vehicle, including oral suspensions.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler Name: [5]
Dr. Masood Homeopathic Pharmaceuticals Private Limited
Labeler Code:
82797
Product Label ID:
1cb79d9c-1de2-3b54-e063-6294a90a667f
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
07-08-2024
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
Flavor(s):
APRICOT (C73363)

Code Structure Chart

Product Details

What is NDC 82797-130?

The NDC code 82797-130 is assigned by the FDA to the product Androtone Syrup which is a human over the counter drug product labeled by Dr. Masood Homeopathic Pharmaceuticals Private Limited. The generic name of Androtone Syrup is tribulus terr, avena sativa, sterculia acum, nuphar lut, sabal serr, agnus cast, lycopodium clav, gentiana lut, yohimbinum, lecithin, natrum phos, kali phos, calcarea phos, natrum mur, strychninum sulph, acidum phos, choloformum. The product's dosage form is syrup and is administered via oral form. The product is distributed in a single package with assigned NDC code 82797-130-12 120 ml in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Androtone Syrup?

Indicated in loss of sex drive and erectile dysfunction.Helpful for those who want to build their muscles.Also increases testosterone levels in the bloodstream

What are Androtone Syrup Active Ingredients?

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.

Which are Androtone Syrup UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Androtone Syrup Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes for Androtone Syrup?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

* Please review the disclaimer below.

Product Footnotes

[1] 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.

[2] 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.

[3] 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".