Find All FDA-Approved Veterinary Drugs, NADA Numbers, Tolerances, Uses, CFR Citations, Approval Dates, Patents and More.
For the marketing executive, the research director and the regulatory affairs manager, the COMPLETE HANDBOOK OF APPROVED NEW ANIMAL DRUG APPLICATIONS IN THE UNITED STATES contains a broad scope of information. It incorporates the more than 1,300 products approved by the Center for Veterinary medicine of the U.S. Food and Drug Administration in a well-indexed manner. And we keep it current quarter by quarter.
AS MANY AS 15 DIFFERENT INFORMATION CATEGORIES
The NADA file number assigned by FDA cross-references each entry to the chapters. The sponsor and brand names tell you who owns the approval and what they call it. The approval date, active ingredient, route of administration and dispensary status is also included. Each product entry lists all approved species, the indications and the directions for use including dosage strengths, cautions and contraindications.
SPECIALIZED INFORMATION FOR SECTION ON NADA FILE NUMBERS
The CFR entry provides the product's applicable Code of Federal Regulations citation along with the sponsor's labeler code.
Each product entry identifies the applicable patent numbers, as published by the FDA, to assist you in generic drug applications.
The tolerance section lists the CFR citations and the drug residue tolerances by tissue for food producing animals.
Each entry for a food-producing animal also lists pre-slaughter withdrawal time, as well as milk discard times.
Specialized chapters on individual species are listed in the referenced sections. A detailed description of the NADA approval process rounds out the book.
The Handbook is divided into chapters by brand name, active ingredient, sponsor firms and by ten different species. All entries are cross-referenced by their NADA number to the main chapter so you can find information - quickly. Please click here for an example of the main chapter.
A constant flow of up-to-date, accurate information on product developments and market changes drives your company. Delivered to you in PDF format on a convenient compact disc, the Handbook offers you a benefit unavailable in any hardbound reference. The Handbook subscription price is $275.00 (domestic) and $300.00 (foreign). This includes the first year of the Quarterly Update Subscription Service. To continue the Quarterly Update Subscription Service beyond the first year, an additional $125.00 (domestic) or $150.00 (foreign) will keep you on top of new and supplemental drug approvals. Every three months you will receive a new CD to replace the outdated one, making your reference the most up-to-date on the market.