NDC 82797-130 Androtone Syrup
Tribulus Terr,Avena Sativa, Sterculia Acum,Nuphar Lut,Sabal Serr,Agnus Cast,Lycopodium - View Dosage, Usage, Ingredients, Routes, UNII
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.
Product Characteristics
Code Structure Chart
Product Details
What is NDC 82797-130?
What are the uses for Androtone Syrup?
What are Androtone Syrup Active Ingredients?
- AVENA SATIVA WHOLE .08 mg/120mL
- CALCIUM PHOSPHATE .005 mg/120mL
- COLA ACUMINATA WHOLE .03 mg/120mL
- GENTIANA LUTEA WHOLE .01 mg/120mL
- LECITHIN, SOYBEAN .0625 mg/120mL
- LYCOPODIUM CLAVATUM WHOLE .01 mg/120mL
- MONOBASIC POTASSIUM PHOSPHATE .005 mg/120mL
- NUPHAR LUTEA WHOLE .03 mg/120mL
- PHOSPHORIC ACID .01 mg/120mL
- SABAL PALMETTO WHOLE .03 mg/120mL
- SODIUM CHLORIDE .005 mg/120mL - A ubiquitous sodium salt that is commonly used to season food.
- SODIUM PHOSPHATE .005 mg/120mL
- STRYCHNINE .015 mg/120mL - An alkaloid found in the seeds of STRYCHNOS NUX-VOMICA. It is a competitive antagonist at glycine receptors and thus a convulsant. It has been used as an analeptic, in the treatment of nonketotic hyperglycinemia and sleep apnea, and as a rat poison.
- TRIBULUS TERRESTRIS WHOLE .08 mg/120mL
- VITEX AGNUS-CASTUS WHOLE .02 mg/120mL
- YOHIMBINE .01 mg/120mL - A plant alkaloid with alpha-2-adrenergic blocking activity. Yohimbine has been used as a mydriatic and in the treatment of ERECTILE DYSFUNCTION.
Which are Androtone Syrup UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRIBULUS TERRESTRIS WHOLE (UNII: 4X4HLN92OT)
- TRIBULUS TERRESTRIS WHOLE (UNII: 4X4HLN92OT) (Active Moiety)
- GENTIANA LUTEA WHOLE (UNII: YFL57437H5)
- GENTIANA LUTEA WHOLE (UNII: YFL57437H5) (Active Moiety)
- YOHIMBINE (UNII: 2Y49VWD90Q)
- YOHIMBINE (UNII: 2Y49VWD90Q) (Active Moiety)
- AVENA SATIVA WHOLE (UNII: 5P8D0Z74RG)
- AVENA SATIVA WHOLE (UNII: 5P8D0Z74RG) (Active Moiety)
- SABAL PALMETTO WHOLE (UNII: ZCM8URO84Q)
- SABAL PALMETTO WHOLE (UNII: ZCM8URO84Q) (Active Moiety)
- VITEX AGNUS-CASTUS WHOLE (UNII: 9HDT03PZ0N)
- VITEX AGNUS-CASTUS WHOLE (UNII: 9HDT03PZ0N) (Active Moiety)
- LYCOPODIUM CLAVATUM WHOLE (UNII: 005ICF6L27)
- LYCOPODIUM CLAVATUM WHOLE (UNII: 005ICF6L27) (Active Moiety)
- CALCIUM PHOSPHATE (UNII: 97Z1WI3NDX)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- COLA ACUMINATA WHOLE (UNII: P4142Q2710)
- COLA ACUMINATA WHOLE (UNII: P4142Q2710) (Active Moiety)
- NUPHAR LUTEA WHOLE (UNII: Z5W3730NWW)
- NUPHAR LUTEA WHOLE (UNII: Z5W3730NWW) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- MONOBASIC POTASSIUM PHOSPHATE (UNII: 4J9FJ0HL51)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- STRYCHNINE (UNII: H9Y79VD43J)
- STRYCHNINE (UNII: H9Y79VD43J) (Active Moiety)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62) (Active Moiety)
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:
- WATER (UNII: 059QF0KO0R)
- SUCROSE (UNII: C151H8M554)
Which are the Pharmacologic Classes for Androtone Syrup?
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Cations, Divalent - [CS]
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
- Potassium Compounds - [CS]
- Potassium Salt - [EPC] (Established Pharmacologic Class)
* Please review the disclaimer below.
[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".