Search Icon

0456-0458 NDC - ARMOUR THYROID (THYROID, PORCINE)

Drug Information

Product NDC: 0456-0458

Proprietary Name: Armour Thyroid

Non Proprietary Name: THYROID, PORCINE

Active Ingredient(s):
  • 30 mg/1 THYROID, PORCINE


Administration Route(s): ORAL

Dosage Form(s): TABLET

Labeler Information

Labeler Name: Allergan, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:4/1/1996

Package Information

No. Package Code Package Description Billing Unit
10456-0458-01100 TABLET in 1 BOTTLE (0456-0458-01)EA
20456-0458-6310 BLISTER PACK in 1 BOX, UNIT-DOSE (0456-0458-63) > 10 TABLET in 1 BLISTER PACK (0456-0458-11)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0456-0458The 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 NAMEHUMAN PRESCRIPTION DRUGIndicates 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.
PROPRIETARY NAMEArmour ThyroidThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMETHYROID, PORCINEThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLETThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE4/1/1996This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct 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 NAMEAllergan, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMETHYROID, PORCINEAn 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 STRENGTH30 
ACTIVE INGRED UNITmg/1 

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 10/18/2022