federal_register: 2013-28394
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| document_number | title | type | abstract | publication_date | pub_year | pub_month | html_url | pdf_url | agency_names | agency_ids | excerpts |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2013-28394 | Draft Guidance for Industry on Bioequivalence Recommendations for Fluticasone Propionate; Salmeterol Xinafoate; Reopening of the Comment Period | Notice | The Food and Drug Administration (FDA) is reopening the comment period for the notice of availability entitled "Draft Guidance for Industry on Bioequivalence Recommendations for Fluticasone Propionate; Salmeterol Xinafoate", published in the Federal Register of September 10, 2013 (78 FR 55263). In that notice, FDA requested public comment on the draft guidance. FDA is reopening the comment period due to the inability of some commenters to submit comments through the www.regulations.gov Web site from November 4, 2013, through November 13, 2013, due to technical difficulties. | 2013-11-27 | 2013 | 11 | https://www.federalregister.gov/documents/2013/11/27/2013-28394/draft-guidance-for-industry-on-bioequivalence-recommendations-for-fluticasone-propionate-salmeterol | https://www.govinfo.gov/content/pkg/FR-2013-11-27/pdf/2013-28394.pdf | Health and Human Services Department; Food and Drug Administration | 221,199 | The Food and Drug Administration (FDA) is reopening the comment period for the notice of availability entitled "Draft Guidance for Industry on Bioequivalence Recommendations for Fluticasone Propionate; Salmeterol Xinafoate", published in the Federal... |