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Animal NDC 86213-133-01 Toltramax Powder 2.5%

2.5% Toltrazuril Powder (25mg/g)

Animal Product Information

Field Name Field Value
Animal NDC Code 86213-133-01
Proprietary Name Toltramax Powder 2.5% 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 2.5% Toltrazuril Powder (25mg/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.

Toltramax Powder 2.5% Images

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