NDC 63304-543-30 - Nefazodone hydrochloride

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: 63304-543
Requested NDC: 63304-543-30
Package NDCs from labels: 63304-543-30, 63304-543-05
Manufacturer: Ranbaxy Pharmaceuticals Inc.
Effective date: 2008-12-24
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Nefazodone hydrochloride - Ranbaxy Pharmaceuticals Inc.	Ranbaxy Pharmaceuticals Inc.	2008-12-24	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63304-543-05	Nefazodone hydrochloride	500 in 1 BOTTLE	TABLET	500		1
63304-543-30	Nefazodone hydrochloride	30 in 1 BOTTLE	TABLET	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63304-543	NEFAZODONE HYDROCHLORIDE TABLET [RANBAXY PHARMACEUTICALS INC.]	1	2 package rows	20090313_b1d149db-ad43-4f3f-aef1-fb0395ba4191.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Nefazodone hydrochloride	ACTIVE INGREDIENT	27X63J94GR	NEFAZODONE HYDROCHLORIDE TABLET [RANBAXY PHARMACEUTICALS INC.]	1
nefazodone	ACTIVE MOIETY	59H4FCV1TF	NEFAZODONE HYDROCHLORIDE TABLET [RANBAXY PHARMACEUTICALS INC.]	1
colloidal silicon dioxide	INACTIVE INGREDIENT	ETJ7Z6XBU4	NEFAZODONE HYDROCHLORIDE TABLET [RANBAXY PHARMACEUTICALS INC.]	1
ferric oxide (red and/or yellow)	INACTIVE INGREDIENT		NEFAZODONE HYDROCHLORIDE TABLET [RANBAXY PHARMACEUTICALS INC.]	1
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	NEFAZODONE HYDROCHLORIDE TABLET [RANBAXY PHARMACEUTICALS INC.]	1
microcrystalline cellulose	INACTIVE INGREDIENT	OP1R32D61U	NEFAZODONE HYDROCHLORIDE TABLET [RANBAXY PHARMACEUTICALS INC.]	1
povidone	INACTIVE INGREDIENT	FZ989GH94E	NEFAZODONE HYDROCHLORIDE TABLET [RANBAXY PHARMACEUTICALS INC.]	1
sodium starch glycolate	INACTIVE INGREDIENT		NEFAZODONE HYDROCHLORIDE TABLET [RANBAXY PHARMACEUTICALS INC.]	1

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 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Nefazodone Hydrochloride	NEFAZODONE HYDROCHLORIDE	Bryant Ranch Prepack	0bd4c34a-4f43-4c84-8b98-1d074cba97d5	2025-09-04	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 1098666
Nefazodone Hydrochloride	NEFAZODONE HYDROCHLORIDE	Teva Pharmaceuticals USA, Inc.	51ff7db5-aaf9-4c3c-86e6-958ebf16b60f	2025-07-31	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 1098649 rxcui: 1098666 rxcui: 1098670 rxcui: 1098674 rxcui: 1098678
5108CA5E-2AFE-5561-02A5-AF90B911698A			b1d149db-ad43-4f3f-aef1-fb0395ba4191	2008-12-24	Boxed warning, Warnings, Adverse reactions	Exact identifier spl id: 5108CA5E-2AFE-5561-02A5-AF90B911698A spl set id: b1d149db-ad43-4f3f-aef1-fb0395ba4191

Reported adverse events (FAERS/openFDA)#

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