NDC 85091-004-17

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
85091-004-17
Product root
85091-004
Identity scope
Package
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
compounderpackage85091-00485091-004-17COMPOUNDEROutsourcing facility compounded drug report2026-12026-09-18
compounderpackage85091-00485091-004-17COMPOUNDEROutsourcing facility compounded drug report2026-12026-10-06

Compounder NDC reports#

Browse the complete compounder directory for this NDC · Browse every current compounder row in the unified auxiliary catalog · browse compounder source captures and parsed snapshots.

Establishment, FEI, Product NDC table
EstablishmentFEIProduct NDCPackage NDCProductActive ingredientsReporting periodNormalization
Apothecary Pharma LLC85091-00485091-004-17Tirzepatide Injection17 mg/1 mL; 1 mg/1 mL2026-1valid
Apothecary Pharma LLC13246226285091-00485091-004-17Tirzepatide; Cyanocobalamin17 mg/1 mL; 1 mg/1 mL2026-1valid

Reported adverse events (FAERS/openFDA)#

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