NDC 84785-0012

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
84785-0012
Product root
84785-0012
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.

Current NDC status page 1 of 1 · 7 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct84785-0012DDiscontinued by firm2026-10-21
excluded packagepackage84785-001284785-0012-1DDiscontinued by firm2026-10-21
excluded packagepackage84785-001284785-0012-2DDiscontinued by firm2026-10-21
excluded packagepackage84785-001284785-0012-3DDiscontinued by firm2026-10-21
excluded packagepackage84785-001284785-0012-4DDiscontinued by firm2026-10-21
excluded packagepackage84785-001284785-0012-5DDiscontinued by firm2026-10-21
excluded packagepackage84785-001284785-0012-6DDiscontinued by firm2026-10-21

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 7 matching rows.

View current auxiliary records. · View the auxiliary file history.

Dataset, Scope, Package NDC table
DatasetScopePackage NDC
excluded productproduct
excluded packagepackage84785-0012-5
excluded packagepackage84785-0012-4
excluded packagepackage84785-0012-2
excluded packagepackage84785-0012-3
excluded packagepackage84785-0012-1
excluded packagepackage84785-0012-6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.