Application 218395

Type: NDA
Sponsor: AZURITY

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	XIFYRM	MELOXICAM	SOLUTION;INTRAVENOUS	30MG/ML (30MG/ML)	Yes	Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
N218395-001	XIFYRM	MELOXICAM	30MG/ML (30MG/ML)	SOLUTION / INTRAVENOUS		RLD, RS	2025-06-05

Orange Book patents#

Current patent rows page 1 of 1 · 1 matching rows.

Application-product, Patent, Expiration table
Application-product	Patent	Expiration	Use code	Coverage / status	Submission date
N218395-001	12263176	2041-07-31		Drug product	2025-06-06

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	RLD / RS	Approval date	Source SHA-256
2026-02-19 14:30 UTC	2026-02	N218395-001	XIFYRM	30MG/ML (30MG/ML)	SOLUTION / INTRAVENOUS	RLD, RS	2025-06-05	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N218395-001	XIFYRM	30MG/ML (30MG/ML)	SOLUTION / INTRAVENOUS	RLD, RS	2025-06-05	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N218395-001	XIFYRM	30MG/ML (30MG/ML)	SOLUTION / INTRAVENOUS	RLD, RS	2025-06-05	`6a471c1ec25d…`
2026-07-26 02:55 UTC · 3 captures of this ZIP	2026-06	N218395-001	XIFYRM	30MG/ML (30MG/ML)	SOLUTION / INTRAVENOUS	RLD, RS	2025-06-05	`a50c72e98297…`

Observed Orange Book patent history#

Captured, Edition, Application-product table
Captured	Edition	Application-product	Patent	Expiration	Coverage / status	Submission date	Source SHA-256
2026-02-19 14:30 UTC	2026-02	N218395-001	12263176	2041-07-31	Drug product	2025-06-06	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N218395-001	12263176	2041-07-31	Drug product	2025-06-06	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N218395-001	12263176	2041-07-31	Drug product	2025-06-06	`6a471c1ec25d…`
2026-07-26 02:55 UTC · 3 captures of this ZIP	2026-06	N218395-001	12263176	2041-07-31	Drug product	2025-06-06	`a50c72e98297…`

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
XIFYRM	MELOXICAM	Azurity Pharmaceuticals, Inc.	bf2b198c-0726-488a-b911-4fe394e4b56e	2025-06-18	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (NDA): 218395 application number: NDA218395

Documents#

Document, Submission type, Date table
Document	Submission type	Date
85828	ORIG	2026-05-05
82481	ORIG	2025-06-06
82478	ORIG	2025-06-06