Animal NDC 86213-142-01 Toltramax Powder 5%

5% Toltrazuril Powder (50 Mg/g)

Field Name	Field Value
Animal NDC Code	86213-142-01
Proprietary Name	Toltramax Powder 5% 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	5% Toltrazuril Powder (50 Mg/g) 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	Vetr, Llc
Product Type	Otc Animal Drug
Active Ingredient(s)	Toltrazuril
Inactive Ingredient(s)	MALTODEXTRIN (7CVR7L4A2D) SILICON DIOXIDE (ETJ7Z6XBU4) MALTODEXTRIN (7CVR7L4A2D) SILICON DIOXIDE (ETJ7Z6XBU4) MALTODEXTRIN (7CVR7L4A2D) SILICON DIOXIDE (ETJ7Z6XBU4) MALTODEXTRIN (7CVR7L4A2D) SILICON DIOXIDE (ETJ7Z6XBU4) MALTODEXTRIN (7CVR7L4A2D) SILICON DIOXIDE (ETJ7Z6XBU4) MALTODEXTRIN (7CVR7L4A2D) SILICON DIOXIDE (ETJ7Z6XBU4)
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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