FDA.reportPublic FDA data

NDC 51672-5273 - 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
51672-5273
Package NDCs from labels
51672-5273-6, 51672-5273-1, 51672-5273-0
Manufacturer
Taro Pharmaceuticals U.S.A., Inc.
Effective date
2009-03-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Citalopram Hydrobromide TabletsTaro Pharmaceuticals U.S.A., Inc.2009-03-16HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51672-5273-0Citalopram Hydrobromide10 in 1 BLISTER PACKTABLET, FILM COATED101
51672-5273-0Citalopram Hydrobromide10 in 1 CARTONTABLET, FILM COATED101
51672-5273-1Citalopram Hydrobromide100 in 1 BOTTLETABLET, FILM COATED1001
51672-5273-6Citalopram Hydrobromide30 in 1 BOTTLETABLET, FILM COATED301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51672-5273CITALOPRAM HYDROBROMIDE TABLET, FILM COATED [TARO PHARMACEUTICALS U.S.A., INC.]14 package rows20090630_C0FCB440-2C9F-4841-B164-5AB7168D81D9.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Citalopram HydrobromideACTIVE INGREDIENTI1E9D14F36CITALOPRAM HYDROBROMIDE TABLET, FILM COATED [TARO PHARMACEUTICALS U.S.A., INC.]1
CitalopramACTIVE MOIETY0DHU5B8D6VCITALOPRAM HYDROBROMIDE TABLET, FILM COATED [TARO PHARMACEUTICALS U.S.A., INC.]1
cellulose, microcrystallineINACTIVE INGREDIENTOP1R32D61UCITALOPRAM HYDROBROMIDE TABLET, FILM COATED [TARO PHARMACEUTICALS U.S.A., INC.]1
hypromelloseINACTIVE INGREDIENT3NXW29V3WOCITALOPRAM HYDROBROMIDE TABLET, FILM COATED [TARO PHARMACEUTICALS U.S.A., INC.]1
magnesium stearateINACTIVE INGREDIENT70097M6I30CITALOPRAM HYDROBROMIDE TABLET, FILM COATED [TARO PHARMACEUTICALS U.S.A., INC.]1
mannitolINACTIVE INGREDIENT3OWL53L36ACITALOPRAM HYDROBROMIDE TABLET, FILM COATED [TARO PHARMACEUTICALS U.S.A., INC.]1
polyethylene glycolINACTIVE INGREDIENT3WJQ0SDW1ACITALOPRAM HYDROBROMIDE TABLET, FILM COATED [TARO PHARMACEUTICALS U.S.A., INC.]1
silicon dioxideINACTIVE INGREDIENTETJ7Z6XBU4CITALOPRAM HYDROBROMIDE TABLET, FILM COATED [TARO PHARMACEUTICALS U.S.A., INC.]1
titanium dioxideINACTIVE INGREDIENT15FIX9V2JPCITALOPRAM HYDROBROMIDE TABLET, FILM COATED [TARO PHARMACEUTICALS U.S.A., 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 5 · 82 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CitalopramCITALOPRAM HYDROBROMIDEREMEDYREPACK INC.0109f365-bebd-4810-a56f-4451e10245db2026-09-04Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 309314
CitalopramCITALOPRAM HYDROBROMIDEREMEDYREPACK INC.625a78b2-4751-4ca5-91b6-7c85fd9f8c2e2026-08-27Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 200371
CitalopramCITALOPRAMREMEDYREPACK INC.f79f878e-99fb-4757-8abb-931af1fa9e2b2026-07-27Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 283672
CitalopramCITALOPRAMREMEDYREPACK INC.aa9c1440-354f-43a6-9e70-fd7bafcb03c52026-07-27Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 309314
CitalopramCITALOPRAMREMEDYREPACK INC.c9809dfe-939e-4f9d-b6dd-f9808fd9f2b12026-07-21Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 309314
CitalopramCITALOPRAMREMEDYREPACK INC.25b0d184-2a4c-42b0-9a57-7a00fa3e0cd72026-07-15Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 200371
CitalopramCITALOPRAMPD-Rx Pharmaceuticals, Inc.9fe40d83-8945-4577-add5-28d52410154e2026-07-07Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 309314
CitalopramCITALOPRAMSt. Mary's Medical Park Pharmacydb900453-4777-4142-a236-5d3a6152d0a52026-06-30Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 200371
CitalopramCITALOPRAMCoupler LLC53e5d66f-7902-76ac-e063-6294a90aa5262026-06-10Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 283672
CitalopramCITALOPRAMCoupler LLC53e6d0a4-95d9-9c1a-e063-6294a90a9d182026-06-10Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 309314
CitalopramCITALOPRAMBryant Ranch Prepack9b53c14c-224c-49ed-8a00-96f871593ab02026-06-04Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 283672
CitalopramCITALOPRAMASCLEMED USA INC.df8db06a-ced7-4dd6-83bd-c61d2f68f1b12026-05-29Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 283672
rxcui: 200371
rxcui: 309314
CitalopramCITALOPRAMSt. Mary's Medical Park Pharmacy351ca54b-0eb6-4e93-8ab4-82fb18dcc9e12026-05-22Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 283672
CitalopramCITALOPRAMQPharma, Inc.f35bfd9e-afb6-409d-a804-6073d812609d2026-05-08Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 200371
CitalopramCITALOPRAMPD-Rx Pharmaceuticals, Inc.43785b49-5d1e-4ae9-b2ff-26be910bde7f2026-05-05Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 200371
CitalopramCITALOPRAMREMEDYREPACK INC.a26772e7-6e4d-489b-bb5e-5bc322ef6dfe2026-05-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 283672
CitalopramCITALOPRAMPD-Rx Pharmaceuticals, Inc.df929b3f-0cda-4a75-96d3-22e6b0edbbc92026-04-29Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 283672
CitalopramCITALOPRAMREMEDYREPACK INC.bdc0c228-797a-42dd-8114-aa68c1eb33002026-04-24Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 200371
CitalopramCITALOPRAMCoupler LLC50380ce5-c77f-3ee3-e063-6394a90a17ae2026-04-24Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 200371
CitalopramCITALOPRAMCardinal Health 107, LLC6c8942f8-963a-4007-a147-b77ac629e4d42026-04-17Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 283672
rxcui: 200371

Reported adverse events (FAERS/openFDA)#

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