federal_register: E9-24882

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts regulation_id_numbers
E9-24882 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 veterinary prescription use of tulathromycin injectable solution for the control of swine respiratory disease (SRD) in groups of pigs where SRD has been diagnosed. 2009-10-16 2009 10 https://www.federalregister.gov/documents/2009/10/16/E9-24882/implantation-or-injectable-dosage-form-new-animal-drugs-tulathromycin https://www.govinfo.gov/content/pkg/FR-2009-10-16/pdf/E9-24882.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 veterinary prescription use of...  

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