NDC 44911-0585-01

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: 44911-0585-01
Product root: 44911-0585
Identity scope: Package
Primary current NDC product row: Not present

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 · 1 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	44911-0585	44911-0585-1	I	Inactivated by FDA		excluded / ndc_excluded.zip	`1332a3947898…`	`d4bfe170f9cd…`

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Joint HP	APIS MELLIFICA, BRYONIA (ALBA), CAUSTICUM, COLCHICUM AUTUMNALE, KALI CARBONICUM, KALMIA LATIFOLIA, LEDUM PALUSTRE, PULSATILLA (PRATENSIS), RHODODENDRON CHRYSANTHUM, RHUS TOX	Energique, Inc.	f65bb6ac-3482-47b1-a678-eff4d130aea1	2024-03-26	Warnings	Exact identifier ndc (product): 44911-0585 ndc11 (package): 44911058501

Reported adverse events (FAERS/openFDA)#

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