NDC 0591-3178 - Citalopram Hydrobromide

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: 0591-3178
Package NDCs from labels: 0591-3178-01, 0591-3178-05, 0591-3178-44
Manufacturer: Contract Pharmacy Services-PA
Effective date: 2010-02-25
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Citalopram Hydrobromide - Contract Pharmacy Services-PA	Contract Pharmacy Services-PA	2010-02-25	HUMAN PRESCRIPTION DRUG LABEL
Citalopram Hydrobromide - Watson Laboratories, Inc	Watson Laboratories, Inc	2008-01-17	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0591-3178-01	Citalopram Hydrobromide	100 in 1 BOTTLE	TABLET	100	4
0591-3178-05	Citalopram Hydrobromide	500 in 1 BOTTLE	TABLET	500	4
0591-3178-44	Citalopram Hydrobromide	100 in 1 BLISTER PACK	TABLET	100	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0591-3178	CITALOPRAM HYDROBROMIDE (CITALOPRAM HYDROBROMIDE) TABLET [WATSON LABORATORIES, INC]	4	3 package rows	20080125_AFA26CDE-E512-48D1-A9AE-3E1CEE2F7F72.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CITALOPRAM HYDROBROMIDE	ACTIVE INGREDIENT	I1E9D14F36	CITALOPRAM HYDROBROMIDE (CITALOPRAM HYDROBROMIDE) TABLET [WATSON LABORATORIES, INC]	4
CITALOPRAM	ACTIVE MOIETY	0DHU5B8D6V	CITALOPRAM HYDROBROMIDE (CITALOPRAM HYDROBROMIDE) TABLET [WATSON LABORATORIES, INC]	4
corn starch	INACTIVE INGREDIENT		CITALOPRAM HYDROBROMIDE (CITALOPRAM HYDROBROMIDE) TABLET [WATSON LABORATORIES, INC]	4
croscarmellose sodium	INACTIVE INGREDIENT		CITALOPRAM HYDROBROMIDE (CITALOPRAM HYDROBROMIDE) TABLET [WATSON LABORATORIES, INC]	4
hypromellose	INACTIVE INGREDIENT		CITALOPRAM HYDROBROMIDE (CITALOPRAM HYDROBROMIDE) TABLET [WATSON LABORATORIES, INC]	4
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	CITALOPRAM HYDROBROMIDE (CITALOPRAM HYDROBROMIDE) TABLET [WATSON LABORATORIES, INC]	4
MANNITOL	INACTIVE INGREDIENT	3OWL53L36A	CITALOPRAM HYDROBROMIDE (CITALOPRAM HYDROBROMIDE) TABLET [WATSON LABORATORIES, INC]	4
microcrystalline cellulose	INACTIVE INGREDIENT		CITALOPRAM HYDROBROMIDE (CITALOPRAM HYDROBROMIDE) TABLET [WATSON LABORATORIES, INC]	4
polyethylene glycol	INACTIVE INGREDIENT		CITALOPRAM HYDROBROMIDE (CITALOPRAM HYDROBROMIDE) TABLET [WATSON LABORATORIES, INC]	4
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	CITALOPRAM HYDROBROMIDE (CITALOPRAM HYDROBROMIDE) TABLET [WATSON LABORATORIES, INC]	4
CITALOPRAM HYDROBROMIDE	ACTIVE INGREDIENT	I1E9D14F36	CITALOPRAM HYDROBROMIDE TABLET [CONTRACT PHARMACY SERVICES-PA]	1
CITALOPRAM	ACTIVE MOIETY	0DHU5B8D6V	CITALOPRAM HYDROBROMIDE TABLET [CONTRACT PHARMACY SERVICES-PA]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	CITALOPRAM HYDROBROMIDE TABLET [CONTRACT PHARMACY SERVICES-PA]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	CITALOPRAM HYDROBROMIDE TABLET [CONTRACT PHARMACY SERVICES-PA]	1
HYPROMELLOSE	INACTIVE INGREDIENT	3NXW29V3WO	CITALOPRAM HYDROBROMIDE TABLET [CONTRACT PHARMACY SERVICES-PA]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	CITALOPRAM HYDROBROMIDE TABLET [CONTRACT PHARMACY SERVICES-PA]	1
MANNITOL	INACTIVE INGREDIENT	3OWL53L36A	CITALOPRAM HYDROBROMIDE TABLET [CONTRACT PHARMACY SERVICES-PA]	1
POLYETHYLENE GLYCOL	INACTIVE INGREDIENT	3WJQ0SDW1A	CITALOPRAM HYDROBROMIDE TABLET [CONTRACT PHARMACY SERVICES-PA]	1
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	CITALOPRAM HYDROBROMIDE TABLET [CONTRACT PHARMACY SERVICES-PA]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	CITALOPRAM HYDROBROMIDE TABLET [CONTRACT PHARMACY SERVICES-PA]	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 40 of 108 · 2,147 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tinted Mineral Lip Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	BASS & KLASS, INC	36add3a3-f1ff-3986-e063-6394a90ab7fe	2025-12-15		Exact identifier unii: 15FIX9V2JP
COOLA BARE REPUBLIC MINERAL SPORT SPF50	TITANIUM DIOXIDE, ZINC OXIDE	COOLA, LLC	bbf15e58-c160-d599-e053-2a95a90a0696	2025-12-14	Warnings	Exact identifier unii: 15FIX9V2JP
Lip Protecting	TITANIUM DIOXIDE, ZINC OXIDE	JOHANNA'S SKIN CARE	3544b8f2-2651-4c01-e063-6394a90ae53d	2025-12-12		Exact identifier unii: 15FIX9V2JP
Tinted SPF40	TITANIUM DIOXIDE, ZINC OXIDE	JOHANNA'S SKIN CARE	3544faa1-ebdf-5dbd-e063-6394a90a7631	2025-12-12		Exact identifier unii: 15FIX9V2JP
Tinted Facial Mineral Sunscreen SPF 40	TITANIUM DIOXIDE, ZINC OXIDE	RSL89 LLC	3531d609-a0d8-cb59-e063-6394a90a4bea	2025-12-12		Exact identifier unii: 15FIX9V2JP
Tinted Facial Mineral Sunscreen SPF 40	TITANIUM DIOXIDE, ZINC OXIDE	RSL89 LLC	3532a6a2-dbb5-8111-e063-6294a90aeaeb	2025-12-12		Exact identifier unii: 15FIX9V2JP
Tinted Daily Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	RSL89 LLC	35338026-525a-d8b3-e063-6394a90a98f5	2025-12-12		Exact identifier unii: 15FIX9V2JP
Mineral Lip Protection	TITANIUM DIOXIDE, ZINC OXIDE	RSL89 LLC	3541971e-3664-a9f5-e063-6294a90ac2d2	2025-12-12		Exact identifier unii: 15FIX9V2JP
Prime Protection Sunscreen non tinted	TITANIUM DIOXIDE, ZINC OXIDE	KRISTI REDD ESTHETICS	36608832-22d8-bc76-e063-6394a90abac6	2025-12-12		Exact identifier unii: 15FIX9V2JP
Prime Protection Sunscreen, tinted	TITANIUM DIOXIDE, ZINC OXIDE	KRISTI REDD ESTHETICS	3660af9e-d60f-c33e-e063-6394a90a3a05	2025-12-12		Exact identifier unii: 15FIX9V2JP
Prime Protection Sunscreen, tinted	TITANIUM DIOXIDE, ZINC OXIDE	KRISTI REDD ESTHETICS	3660e701-1373-eef4-e063-6394a90a6140	2025-12-12		Exact identifier unii: 15FIX9V2JP
sheer tinted sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	SARA ELIZABETH SKINCARE	3b177c49-ed8c-42b9-e063-6294a90a82c6	2025-12-12	Warnings	Exact identifier unii: 15FIX9V2JP
Non-Tinted Matte Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Skin Philosophy by Kelly	3581ab49-ef55-3743-e063-6394a90a3bd5	2025-12-12		Exact identifier unii: 15FIX9V2JP
Matte Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Skin Philosophy by Kelly	3581cf33-3520-42f7-e063-6394a90a6f93	2025-12-12		Exact identifier unii: 15FIX9V2JP
Matte Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Skin Philosophy by Kelly	3592b2c7-295a-7c60-e063-6394a90a387b	2025-12-12		Exact identifier unii: 15FIX9V2JP
Sun Elegant Mineral Sunscreen Tinted	TITANIUM DIOXIDE, ZINC OXIDE	SKIN BY NESRIN	3580ae10-1867-cb68-e063-6394a90a72df	2025-12-12		Exact identifier unii: 15FIX9V2JP
PROTECTOR SOLAR NON-TINTED SPF SUNSCREEN	TITANIUM DIOXIDE, ZINC OXIDE	The Beez Kneez Skin Care & Acne Clinic LLC	358195c0-6d28-1ffe-e063-6394a90a6027	2025-12-12		Exact identifier unii: 15FIX9V2JP
Matte Velvet Tint	TITANIUM DIOXIDE, ZINC OXIDE	Brent Loftis, D.O., Inc., A California Medical Corporation	3583f860-664b-2658-e063-6394a90a3857	2025-12-12		Exact identifier unii: 15FIX9V2JP
SPF Lip	TITANIUM DIOXIDE, ZINC OXIDE	Brent Loftis, D.O., Inc., A California Medical Corporation	359297cd-10e2-6ddd-e063-6394a90a4aa0	2025-12-12		Exact identifier unii: 15FIX9V2JP
Matte Velvet Tint	TITANIUM DIOXIDE, ZINC OXIDE	Brent Loftis, D.O., Inc., A California Medical Corporation	359641c5-0e19-f243-e063-6394a90aeebc	2025-12-12		Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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