federal_register: 2012-6544

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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
2012-6544 Oral Dosage Form New Animal Drugs; Pergolide Rule The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of an original new animal drug application (NADA) filed by Boehringer Ingelheim Vetmedica, Inc. The NADA provides for the veterinary prescription use of pergolide mesylate tablets in horses for the control of clinical signs associated with Pituitary Pars Intermedia Dysfunction (Equine Cushing's Disease). 2012-03-19 2012 3 https://www.federalregister.gov/documents/2012/03/19/2012-6544/oral-dosage-form-new-animal-drugs-pergolide https://www.govinfo.gov/content/pkg/FR-2012-03-19/pdf/2012-6544.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 an original new animal drug application (NADA) filed by Boehringer Ingelheim Vetmedica, Inc. The NADA provides for the veterinary prescription use of...  

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