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 47 of 108 · 2,147 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mineral Sunscreen Dry Touch NT	TITANIUM DIOXIDE, ZINC OXIDE	Cutis Wellness Dermatology And Dermatopathology PLLC	334ffc49-3196-0995-e063-6394a90ad559	2025-12-09		Exact identifier unii: 15FIX9V2JP
Foam Weightless Sunscreen Non-Tinted Drytouch NT	TITANIUM DIOXIDE, ZINC OXIDE	Cutis Wellness Dermatology And Dermatopathology PLLC	335ec22c-6a9a-c4d1-e063-6394a90ac0b0	2025-12-09		Exact identifier unii: 15FIX9V2JP
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Lily Lee, MD	323356ea-31a0-6ff0-e063-6294a90a135c	2025-12-09		Exact identifier unii: 15FIX9V2JP
Non-Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Lily Lee, MD	32330376-5db0-202b-e063-6294a90add15	2025-12-09		Exact identifier unii: 15FIX9V2JP
Sunscreen Plus Mineral Stick Untinted	TITANIUM DIOXIDE, ZINC OXIDE	Lily Lee, MD	3234b498-5b56-55f4-e063-6294a90a9b87	2025-12-09		Exact identifier unii: 15FIX9V2JP
Sunscreen Plus Mineral Stick Tinted	TITANIUM DIOXIDE, ZINC OXIDE	Lily Lee, MD	32351db0-884c-8fa0-e063-6294a90acba2	2025-12-09		Exact identifier unii: 15FIX9V2JP
Sheer Satin Mineral Sunscreen Tinted	TITANIUM DIOXIDE, ZINC OXIDE	INTEGRATIVE AESTHETICS BOSTON, LLC	3143d8b0-4af8-f52d-e063-6294a90a926b	2025-12-09	Warnings	Exact identifier unii: 15FIX9V2JP
Sheer Non-Tinted Mineral Sunscreen Stick	TITANIUM DIOXIDE, ZINC OXIDE	Face Collection, L.L.C.	33d83cfb-045d-141c-e063-6394a90a2e04	2025-12-09		Exact identifier unii: 15FIX9V2JP
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Maloney Plastic Surgery Skin Care, PLLC	316b7584-c782-fe9e-e063-6394a90a76fe	2025-12-09		Exact identifier unii: 15FIX9V2JP
Transparent Tinted Mineral Sunscreen Stick	TITANIUM DIOXIDE, ZINC OXIDE	Face Collection, L.L.C.	33dbfd9b-b90f-bb32-e063-6294a90af7dc	2025-12-09		Exact identifier unii: 15FIX9V2JP
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Maloney Plastic Surgery Skin Care, PLLC	316b46ac-6dde-72d1-e063-6294a90a03da	2025-12-09		Exact identifier unii: 15FIX9V2JP
BIOJUVE Microbiome-Safe Sheer Finish SPF 50 Sunscreen	TITANIUM DIOXIDE AND ZINC OXIDE	Crown Laboratories	ece7565b-f3e5-3386-e053-2a95a90a5802	2025-12-09	Warnings	Exact identifier unii: 15FIX9V2JP
Florida Babe Sport Non-Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Tichy Anesthesia PA	31e4756d-8604-6e75-e063-6294a90aebe1	2025-12-09		Exact identifier unii: 15FIX9V2JP
Florida Babe Sport Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Tichy Anesthesia PA	31e4d9ae-f532-f9f5-e063-6294a90a8d39	2025-12-09		Exact identifier unii: 15FIX9V2JP
Florida Babe SPORT Mineral Sunscreen Stick Tinted	TITANIUM DIOXIDE, ZINC OXIDE	Tichy Anesthesia PA	31f5bbe4-5f6e-3bef-e063-6294a90a2646	2025-12-09		Exact identifier unii: 15FIX9V2JP
Florida Babe SPORT Mineral Sunscreen Stick Non-Tinted	TITANIUM DIOXIDE, ZINC OXIDE	Tichy Anesthesia PA	31f54a79-70b7-def5-e063-6294a90a709b	2025-12-09		Exact identifier unii: 15FIX9V2JP
Florida Babe Sport Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Tichy Anesthesia PA	3231b71c-4d27-e5e2-e063-6294a90a031b	2025-12-09		Exact identifier unii: 15FIX9V2JP
Arbonne Soft Focus Veil Broad Spectrum SPF 30 Sunscreen	TITANIUM DIOXIDE AND ZINC OXIDE	Arbonne International, LLC	3c9b605b-5a16-4f89-a956-8c4c62de72d3	2025-12-09	Warnings	Exact identifier unii: 15FIX9V2JP
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	THE AESTHETICS ACADEMY, LLC	364b9560-f7a1-ed8f-e063-6294a90a2c41	2025-12-09		Exact identifier unii: 15FIX9V2JP
SCALP SUNSCREEN	TITANIUM DIOXIDE, ZINC OXIDE	FOLICULE LLC	387b10e1-5443-7b7a-e063-6394a90a2c7a	2025-12-09		Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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