58198-0329 NDC - PROGESTERONE, ESTRADIOL BENZOATE AND TYLOSIN TARTRATE

Drug Information

  • Product NDC: 58198-0329
  • Proprietary Name:
  • Non Proprietary Name: progesterone, estradiol benzoate and tylosin tartrate
  • Active Ingredient(s): 20 mg/1 ESTRADIOL BENZOATE; 200 mg/1 PROGESTERONE; 29 mg/1 TYLOSIN TARTRATE
  • Administration Route(s):
  • Dosage Form(s): IMPLANT

Labeler Information

Field Name Field Value
Labeler Name: Elanco US Inc.
Product Type: DRUG FOR FURTHER PROCESSING
FDA Application Number:
Marketing Category: EXPORT ONLY
Start Marketing Date:11/7/2001

Package Information

No. Package Code Package Description Billing Unit
158198-0329-15 POUCH in 1 CARTON (58198-0329-1) / 1 CARTRIDGE in 1 POUCH / 20 IMPLANT in 1 CARTRIDGE

NDC Record

Field Name Field Value Definition
PRODUCT NDC58198-0329The 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 NAMEDRUG FOR FURTHER PROCESSINGIndicates 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 NAMEprogesterone, estradiol benzoate and tylosin tartrateThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEIMPLANTThe translation of the dosage form Code submitted by the firm.
START MARKETING DATE11/7/2001This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEEXPORT ONLYProduct 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 NAMEElanco US Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEESTRADIOL BENZOATE; PROGESTERONE; TYLOSIN TARTRATEAn 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 STRENGTH20; 200; 29 
ACTIVE INGRED UNITmg/1; mg/1; mg/1 

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

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