NDC 72682-2230

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
72682-2230
Product root
72682-2230
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 · 4 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
compounderpackage72682-223072682-2230-1COMPOUNDEROutsourcing facility compounded drug report2024-12026-10-21
compounderpackage72682-223072682-2230-3COMPOUNDEROutsourcing facility compounded drug report2023-12026-10-21
compounderpackage72682-223072682-2230-3COMPOUNDEROutsourcing facility compounded drug report2022-22026-10-21
compounderpackage72682-223072682-2230-3COMPOUNDEROutsourcing facility compounded drug report2022-12026-10-21

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 · 8 matching rows.

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

Captured / source date, Package NDC, Reporting period table
Captured / source datePackage NDCReporting periodSnapshotSource SHA-256
2025-12-16 00:49 UTC · source 2025-09-2572682-2230-12024-13f6f48d8db7b…6316a3eebc6a…
2025-08-27 00:00 UTC · source 2025-08-2072682-2230-12024-1af8e9b524e63…ca326a94a5e9…
2025-08-27 00:00 UTC · source 2025-08-2072682-2230-32023-1af8e9b524e63…ca326a94a5e9…
2025-08-27 00:00 UTC · source 2025-08-2072682-2230-32022-2af8e9b524e63…ca326a94a5e9…
2025-08-27 00:00 UTC · source 2025-08-2072682-2230-32022-1af8e9b524e63…ca326a94a5e9…
2025-01-13 04:20 UTC · source 2024-11-2072682-2230-12024-185f958c8d153…997044a9741e…
2025-01-13 04:20 UTC · source 2024-11-2072682-2230-32023-185f958c8d153…997044a9741e…
2025-01-13 04:20 UTC · source 2024-11-2072682-2230-32022-285f958c8d153…997044a9741e…

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
AnazaoHealth Corporation79669261972682-223072682-2230-1Riboflavin; Niacinamide; Dexpanthenol; Pyridoxine; Thiamine Hydrochloride2 mg/1 mL; 75 mg/1 mL; 6.6 mg/1 mL; 2 mg/1 mL; 75 mg/1 mL2024-1valid
AnazaoHealth Corporation79669261972682-223072682-2230-3Riboflavin; Niacinamide; Dexpanthenol; Pyridoxine; Thiamine Hydrochloride2 mg/1 mL; 75 mg/1 mL; 6.6 mg/1 mL; 2 mg/1 mL; 75 mg/1 mL2023-1valid
AnazaoHealth Corporation79669261972682-223072682-2230-3Riboflavin; Niacinamide; Dexpanthenol; Pyridoxine; Thiamine Hydrochloride2 mg/1 mL; 75 mg/1 mL; 6.6 mg/1 mL; 2 mg/1 mL; 75 mg/1 mL2022-2valid
AnazaoHealth Corporation79669261972682-223072682-2230-3Riboflavin; Niacinamide; Dexpanthenol; Pyridoxine; Thiamine Hydrochloride2 mg/1 mL; 75 mg/1 mL; 6.6 mg/1 mL; 2 mg/1 mL; 75 mg/1 mL2022-1valid

Reported adverse events (FAERS/openFDA)#

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