federal_register: 2012-1744
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2012-1744 | Oral Dosage Form New Animal Drugs; Milbemycin Oxime, Lufenuron, and Praziquantel | Rule | The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a new animal drug application (NADA) filed by Novartis Animal Health US, Inc. The NADA provides for the veterinary prescription use of milbemycin oxime, lufenuron, and praziquantel for the prevention of heartworm disease, for prevention and control of fleas, and for the treatment and control of various internal parasites in dogs. | 2012-01-27 | 2012 | 1 | https://www.federalregister.gov/documents/2012/01/27/2012-1744/oral-dosage-form-new-animal-drugs-milbemycin-oxime-lufenuron-and-praziquantel | https://www.govinfo.gov/content/pkg/FR-2012-01-27/pdf/2012-1744.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 new animal drug application (NADA) filed by Novartis Animal Health US, Inc. The NADA provides for the veterinary prescription use of milbemycin... |