federal_register: E8-1906

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts
E8-1906 Implantation or Injectable Dosage Form New Animal Drugs; Tulathromycin Rule The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a supplemental new animal drug application (NADA) filed by Pfizer, Inc. The supplemental NADA provides for veterinarian prescription use of tulathromycin injectable solution for the treatment of infectious bovine keratoconjunctivitis and the addition of a pathogen to the indication for use for treatment of swine respiratory disease. 2008-02-01 2008 2 https://www.federalregister.gov/documents/2008/02/01/E8-1906/implantation-or-injectable-dosage-form-new-animal-drugs-tulathromycin https://www.govinfo.gov/content/pkg/FR-2008-02-01/pdf/E8-1906.pdf Health and Human Services Department; Food and Drug Administration 221,199 The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a supplemental new animal drug application (NADA) filed by Pfizer, Inc. The supplemental NADA provides for veterinarian prescription use of...

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