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Animal NDC 86216-007-01 Goat Dewormer

Fenbendazole

Animal Product Information

Field Name Field Value
Animal NDC Code 86216-007-01
Proprietary Name Goat Dewormer What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name Fenbendazole 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.
Labeler Name Pet Professional Inc.
Product Type Otc Animal Drug
Active Ingredient(s)
  • Fenbendazole
Inactive Ingredient(s)
  • WATER (059QF0KO0R)
  • WATER (059QF0KO0R)
Marketing Category UNAPPROVED DRUG OTHER 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.

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Goat Dewormer Animal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Direction



Calculate the correct dose based on estimated body weight. Recommended dose: 2.3 mg/lb, equivalent to 2.3 mL per 100 lb body weight.

Oral administration via syringe or drencher.

Use measuring cup or syringe for accuracy.

Administer slowly to avoid aspiration.

Repeat dose after 5-6 weeks if heavyinfestation.


* The information on this page is for an ANIMAL PRODUCT, please review the complete disclaimer below.