NDC 72627-2409

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
72627-2409
Product root
72627-2409
Identity scope
Product
Primary current NDC product row
Not present

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

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

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
compounderpackage72627-240972627-2409-2COMPOUNDEROutsourcing facility compounded drug report2019-12026-08-01

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
Empower Pharmacy83117894772627-240972627-2409-2.gamma.-Aminobutyric Acid; Magnesium Chloride Tetrahydrate; Taurine; Theanine50 mg/1 mL; 50 mg/1 mL; 50 mg/1 mL; 50 mg/1 mL2019-1valid