NDC 84019-301

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: 84019-301
Product root: 84019-301
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 · 12 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	84019-301		I	Inactivated by FDA	2026-10-05
excluded package	package	84019-301	84019-301-01	I	Inactivated by FDA	2026-10-05
excluded package	package	84019-301	84019-301-02	I	Inactivated by FDA	2026-10-05
excluded package	package	84019-301	84019-301-03	I	Inactivated by FDA	2026-10-05
excluded package	package	84019-301	84019-301-04	I	Inactivated by FDA	2026-10-05
excluded package	package	84019-301	84019-301-05	I	Inactivated by FDA	2026-10-05
excluded package	package	84019-301	84019-301-06	I	Inactivated by FDA	2026-10-05
excluded package	package	84019-301	84019-301-07	I	Inactivated by FDA	2026-10-05
excluded package	package	84019-301	84019-301-08	I	Inactivated by FDA	2026-10-05
excluded package	package	84019-301	84019-301-09	I	Inactivated by FDA	2026-10-05
excluded package	package	84019-301	84019-301-10	I	Inactivated by FDA	2026-10-05
excluded package	package	84019-301	84019-301-11	I	Inactivated by FDA	2026-10-05

Reported adverse events (FAERS/openFDA)#

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