federal_register: E9-29583
This data as json
| document_number | title | type | abstract | publication_date | pub_year | pub_month | html_url | pdf_url | agency_names | agency_ids | excerpts | regulation_id_numbers |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| E9-29583 | Implantation or Injectable Dosage Form New Animal Drugs; Insulin | 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 veterinary prescription use of an injectable suspension of protamine zinc recombinant human insulin for the reduction of hyperglycemia and hyperglycemia-associated clinical signs in cats with diabetes mellitus. | 2009-12-14 | 2009 | 12 | https://www.federalregister.gov/documents/2009/12/14/E9-29583/implantation-or-injectable-dosage-form-new-animal-drugs-insulin | https://www.govinfo.gov/content/pkg/FR-2009-12-14/pdf/E9-29583.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 veterinary prescription use of an... |