NDC 70518-4335-01 - Citalopram

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
70518-4335
Requested NDC
70518-4335-01
Package NDCs from labels
70518-4335-0, 70518-4335-1, 70518-4335-2, 70518-4335-4, 70518-4335-3, 70518-4335-01
Manufacturer
REMEDYREPACK INC.
Effective date
2026-04-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Citalopram - REMEDYREPACK INC.REMEDYREPACK INC.2026-04-24HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-4335-0Citalopram30 in 1 BLISTER PACKTABLET, FILM COATED304
70518-4335-1Citalopram90 in 1 BOTTLE, PLASTICTABLET, FILM COATED904
70518-4335-2Citalopram30 in 1 BLISTER PACKTABLET, FILM COATED304
70518-4335-3Citalopram50 in 1 BOXTABLET, FILM COATED504
70518-4335-4Citalopram1 in 1 POUCHTABLET, FILM COATED14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-4335CITALOPRAM TABLET, FILM COATED [REMEDYREPACK INC.]1Current NDC, 5 package rows20250503_bdc0c228-797a-42dd-8114-aa68c1eb3300.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 3 of 5 · 88 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CitalopramCITALOPRAM HYDROBROMIDEBryant Ranch Prepack0bc0e09e-0f1d-4d52-b8fe-3ef8a2e5ea522025-06-11Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 200371
unii: I1E9D14F36
Citalopram HydrobromideCITALOPRAM HYDROBROMIDEATLANTIC BIOLOGICALS CORP.2640311d-8b88-4513-9c80-a08390b8142a2025-05-12Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I1E9D14F36
Citalopram HydrobromideCITALOPRAM HYDROBROMIDENuCare Pharmaceuticals,Inc.c577b306-ee7c-8364-e053-2a95a90abb132025-01-23Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA078216
rxcui: 283672
unii: I1E9D14F36
CITALOPRAMCITALOPRAMGolden State Medical Supply, Inc.f3a26d92-b662-4896-82eb-2619480424082025-01-14Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 283672
rxcui: 200371
rxcui: 309314
unii: I1E9D14F36
CitalopramCITALOPRAMPD-Rx Pharmaceuticals, Inc.75f6db65-e4ed-470a-9e56-12791f22ee9b2025-01-07Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 200371
unii: I1E9D14F36
Citalopram HydrobromideCITALOPRAM HYDROBROMIDENuCare Pharmaceuticals,Inc.c584909b-e7b2-7108-e053-2995a90a2f542024-12-31Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA078216
rxcui: 200371
unii: I1E9D14F36
CitalopramCITALOPRAMAdvanced Rx of Tennessee, LLCb3541f26-dc8d-6591-e053-2995a90a23d92024-12-31Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA078216
rxcui: 200371
unii: I1E9D14F36
Citalopram HydrobromideCITALOPRAM HYDROBROMIDEAdvanced Rx Pharmacy of Tennessee, LLCf8b06b55-f6a2-2438-e053-6394a90a530a2024-12-31Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 283672
unii: I1E9D14F36
Citalopram HydrobromideCITALOPRAM HYDROBROMIDEQuality Care Products, LLC6fc110ba-87e7-404e-9e00-b680f354c7b02024-12-18Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA078216
rxcui: 200371
unii: I1E9D14F36
Citalopram HydrobromideCITALOPRAM HYDROBROMIDEQuality Care Products, LLCe22fe468-5d9e-4ec7-a69b-4988e0b8acbd2024-12-18Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA078216
rxcui: 283672
unii: I1E9D14F36
Citalopram HydrobromideCITALOPRAM HYDROBROMIDEBryant Ranch Prepack8719bd44-36b6-468d-9203-8c53a26451842024-11-08Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA078216
rxcui: 200371
unii: I1E9D14F36
Citalopram HydrobromideCITALOPRAM HYDROBROMIDEProficient Rx LP1a136cc3-d655-4f3c-8710-2603dc0084922024-11-01Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA078216
rxcui: 283672
rxcui: 200371
unii: I1E9D14F36
CitalopramCITALOPRAM HYDROBROMIDEA-S Medication Solutions2500cc9d-a67d-46c5-9a76-99bc63959d672024-10-30Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 283672
unii: I1E9D14F36
Citalopram HydrobromideCITALOPRAM HYDROBROMIDEBryant Ranch Prepack15cb00da-4435-4930-90d0-faadf2739a5c2024-10-30Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA078216
rxcui: 309314
unii: I1E9D14F36
CitalopramCITALOPRAMBryant Ranch Prepack2a8acad8-0ba0-4631-9f6d-f587e7a8558c2024-10-04Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 309314
unii: I1E9D14F36
CitalopramCITALOPRAMAmneal Pharmaceuticals LLC6a402640-1c9d-4fca-8b5b-e1ac1dd4ca5a2024-09-23Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 283672
rxcui: 200371
rxcui: 309314
unii: I1E9D14F36
Citalopram HydrobromideCITALOPRAM HYDROBROMIDEA-S Medication Solutions05421bee-f746-418e-bb9c-ab44a89b567d2024-09-18Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA078216
rxcui: 283672
rxcui: 200371
rxcui: 309314
unii: I1E9D14F36
CITALOPRAMCITALOPRAMEpic Pharma, LLC08b6d5da-5919-4760-9e16-3b478a14d6d72024-09-18Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 283672
rxcui: 200371
rxcui: 309314
unii: I1E9D14F36
CitalopramCITALOPRAM HYDROBROMIDEA-S Medication Solutionsb244d4eb-8311-4663-8bca-dc08e88e5f5d2024-08-21Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 309314
unii: I1E9D14F36
CitalopramCITALOPRAMCipla USA Inc.0580559a-783a-4a0a-8d81-ee30a29077c52024-08-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 283672
rxcui: 200371
rxcui: 309314
unii: I1E9D14F36

Reported adverse events (FAERS/openFDA)#

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