NDC 63629-4989-01 - Wixela Inhub

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 63629-4989
Requested NDC: 63629-4989-01
Package NDCs from labels: 63629-4989-1, 63629-4989-01
Manufacturer: Bryant Ranch Prepack
Effective date: 2025-02-13
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Wixela Inhub - Bryant Ranch Prepack	Bryant Ranch Prepack	2025-02-13	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63629-4989-1	Wixela Inhub	60 in 1 INHALER	POWDER	60		100
63629-4989-1	Wixela Inhub	1 in 1 CARTON	POWDER	1		100

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63629-4989	WIXELA INHUB (FLUTICASONE PROPIONATE AND SALMETEROL) POWDER [BRYANT RANCH PREPACK]	100	Current NDC, 2 package rows	20250215_6a5e28ef-3bbb-43a6-b599-499b3c6076c9.zip

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 9 of 9 · 161 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Fluticasone Propionate	FLUTICASONE PROPIONATE	Allegiant Health	4e1cd546-4598-115b-0357-5d0c22731faa	2017-11-17	Warnings	Exact identifier unii: O2GMZ0LF5W

Reported adverse events (FAERS/openFDA)#

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