FDA guidance
ANDA Submissions - Refuse-to-Receive Standards: Questions and Answers Guidance for…
FDA guidance · Draft · issued Oct 3, 2017
Key facts
| Title | ANDA Submissions - Refuse-to-Receive Standards: Questions and Answers Guidance for Industry |
|---|---|
| Status | Draft |
| Issue date | Oct 3, 2017 |
| Center | Center for Drug Evaluation and Research |
| Issuing office | Center for Drug Evaluation and Research |
| Communication type | Guidance Document |
| Regulated product | Drugs |
| Topics | User Fees |
| Docket number | FDA-2017-D-5846 |
| Comments close | Jan 2, 2018 |
| Open for comment | No |
| Document on fda.gov | fda.gov |
At a glance
- None Product codes referenced
- None Recognized standards referenced
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA guidance documents
FDA guidance documents describe the agency's current thinking on regulatory topics. Drafts are issued for comment before a final version is published.
Source: U.S. Food and Drug Administration (FDA), Guidance Documents