83162-001 NDC - THYROID POWDER

Drug Information

  • Product NDC: 83162-001
  • Proprietary Name:
  • Non Proprietary Name: Thyroid Powder
  • Active Ingredient(s): 1 g/g THYROID, UNSPECIFIED
  • Administration Route(s):
  • Dosage Form(s): POWDER

Labeler Information

Field Name Field Value
Labeler Name: Xenova Sciences, LLC
Product Type: BULK INGREDIENT
FDA Application Number:
Marketing Category: BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Start Marketing Date:10/1/2023

Package Information

No. Package Code Package Description Billing Unit
183162-001-011 BAG in 1 JAR (83162-001-01) / 200 g in 1 BAG
283162-001-021 BAG in 1 JAR (83162-001-02) / 1000 g in 1 BAG
383162-001-032 BAG in 1 DRUM (83162-001-03) / 29483.5 g in 1 BAG
483162-001-041 BAG in 1 DRUM (83162-001-04) / 58967 g in 1 BAG
583162-001-051 BAG in 1 JAR (83162-001-05) / 25 g in 1 BAG
683162-001-061 BAG in 1 JAR (83162-001-06) / 50 g in 1 BAG
783162-001-071 BAG in 1 JAR (83162-001-07) / 100 g in 1 BAG
883162-001-081 BAG in 1 JAR (83162-001-08) / 500 g in 1 BAG

NDC Record

Field Name Field Value Definition
PRODUCT NDC83162-001The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEBULK INGREDIENTIndicates 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.
NON PROPRIETARY NAMEThyroid PowderThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPOWDERThe translation of the dosage form Code submitted by the firm.
START MARKETING DATE10/1/2023This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEBULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDINGProduct 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.
LABELER NAMEXenova Sciences, LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMETHYROID, UNSPECIFIEDAn 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.
ACTIVE NUMERATOR STRENGTH1 
ACTIVE INGRED UNITg/g 

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This page was last updated on: 12/6/2025

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