NDC 26436-5604

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: 26436-5604
Product root: 26436-5604
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
compounder	package	26436-5604	26436-5604-2	COMPOUNDER	Outsourcing facility compounded drug report	2024-2	2025-09-25
compounder	package	26436-5604	26436-5604-2	COMPOUNDER	Outsourcing facility compounded drug report	2024-2	2026-08-01

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
Establishment	FEI	Product NDC	Package NDC	Product	Active ingredients	Reporting period	Normalization
Hybrid Pharma		26436-5604	26436-5604-2	Ethanol	95 mL/100 mL	2024-2	valid
Hybrid Pharma	079665742	26436-5604	26436-5604-2	Alcohol	95 mL/100 mL	2024-2	valid