NDC 84778-091
This exact product or package identity exists in FDA auxiliary data but is not present in the current primary NDC product table. The package identity is preserved; status rows are reported source observations, not medical conclusions.
- Requested NDC
- 84778-091
- Product root
- 84778-091
- Identity scope
- Product
- Primary current NDC product row
- Not present
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 84778-091 | I | Inactivated by FDA | 2026-10-05 | ||
| excluded package | package | 84778-091 | 84778-091-01 | I | Inactivated by FDA | 2026-10-05 | |
| excluded package | package | 84778-091 | 84778-091-02 | I | Inactivated by FDA | 2026-10-05 | |
| excluded package | package | 84778-091 | 84778-091-03 | I | Inactivated by FDA | 2026-10-05 | |
| excluded package | package | 84778-091 | 84778-091-04 | I | Inactivated by FDA | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.