Regulations.gov document
Tab 3 - 72 FR 30386 - "Draft Guidances for Industry Describing Product-Specific…
Supporting & Related Material · FDA-2007-P-0010 · posted Jun 21, 2009
Key facts
| Document ID | FDA-2007-P-0010-0018 |
|---|---|
| Title | Tab 3 - 72 FR 30386 - "Draft Guidances for Industry Describing Product-Specific Bioequivalence Recommendations; Availability" - [Axcan Pharma US, Inc. - Supplement Citizen Petition] |
| Document type | Supporting & Related Material |
| Subtype | SUP-Supplement (Supporting and Related Material) |
| Agency | FDA |
| Docket | FDA-2007-P-0010 |
| Posted | Jun 21, 2009 |
| Effective date | Jun 16, 2009 |
At a glance
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