NDC 70004-001-22

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: 70004-001-22
Product root: 70004-001
Identity scope: Package
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
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
compounder	package	70004-001	70004-001-22	COMPOUNDER	Outsourcing facility compounded drug report	2020-2	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
SCA Pharmaceuticals, LLC	080545245	70004-001	70004-001-22	Acetaminophen	10 mg/1 mL	2020-2	valid
SCA Pharmaceuticals, LLC	080545245	70004-001	70004-001-28	Acetaminophen	10 mg/1 mL	2020-2	valid
SCA Pharmaceuticals, LLC	080545245	70004-001	70004-001-56	Acetaminophen	10 mg/1 mL	2020-2	valid