FDA.reportPublic FDA data

NDC 70518-2195-01 - Torsemide

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
70518-2195
Requested NDC
70518-2195-01
Package NDCs from labels
70518-2195-0, 70518-2195-1, 70518-2195-01
Manufacturer
REMEDYREPACK INC.
Effective date
2026-07-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Torsemide - REMEDYREPACK INC.REMEDYREPACK INC.2026-07-21HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2023-03-08These highlights do not include all the information needed to use TORSEMIDE TABLETS safely and effectively. See full prescribing information for TORSEMIDE TABLETS. TORSEMIDE tablets, for oral use Initial U.S. Approval: 1993
2023-03-08These highlights do not include all the information needed to use TORSEMIDE TABLETS safely and effectively. See full prescribing information for TORSEMIDE TABLETS. TORSEMIDE tablets, for oral use Initial U.S. Approval: 1993
2023-01-30These highlights do not include all the information needed to use TORSEMIDE TABLETS safely and effectively. See full prescribing information for TORSEMIDE TABLETS. TORSEMIDE tablets, for oral use Initial U.S. Approval: 1993
2023-01-30These highlights do not include all the information needed to use TORSEMIDE TABLETS safely and effectively. See full prescribing information for TORSEMIDE TABLETS. TORSEMIDE tablets, for oral use Initial U.S. Approval: 1993

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-2195-0Torsemide90 in 1 BOTTLE, PLASTICTABLET906
70518-2195-1Torsemide90 in 1 BOTTLE, PLASTICTABLET906

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 4 of 5 · 94 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TorsemideTORSEMIDEGolden State Medical Supply, Inc.2411e6f8-4fc3-f986-e063-6294a90a055a2024-10-09Warnings, Adverse reactionsExact identifier
unii: W31X2H97FB
TorsemideTORSEMIDEA-S Medication Solutions05c8a6ee-9517-453f-8dd6-7e5ca83c5a682024-10-01Warnings, Adverse reactionsExact identifier
rxcui: 198371
unii: W31X2H97FB
TorsemideTORSEMIDENCS HealthCare of KY, LLC dba Vangard Labs99b537f3-1fbf-48b7-ac3e-0a43e6aab3132024-09-30Warnings, Adverse reactionsExact identifier
unii: W31X2H97FB
TorsemideTORSEMIDEXLCare Pharmaceuticals Inc.234ff9d7-a02e-417f-a1f9-94038783cc772024-09-10Warnings, Adverse reactionsExact identifier
rxcui: 198371
unii: W31X2H97FB
TorsemideTORSEMIDEBryant Ranch Prepack13d851b6-3355-4541-93e8-73cdaf0f13d12024-07-16Warnings, Adverse reactionsExact identifier
unii: W31X2H97FB
Artificial TearsPOLYVINYL ALCOHOL, POVIDONENuCare Pharmaceuticals,Inc.9c1c4911-908e-3c3c-e053-2995a90abcfc2024-06-14WarningsExact identifier
unii: FZ989GH94E
TorsemideTORSEMIDEAurobindo Pharma Limited55e88727-864e-4313-860c-31a6ca45168f2024-05-08Warnings, Adverse reactionsExact identifier
rxcui: 198371
unii: W31X2H97FB
TorsemideTORSEMIDERising Pharma Holdings, Inc.3c8f1c0b-8a44-4ca0-b2cf-3c591f8878fd2024-05-08Warnings, Adverse reactionsExact identifier
rxcui: 198371
unii: W31X2H97FB
TorsemideTORSEMIDEAphena Pharma Solutions - Tennessee, LLC159e8c90-ebc6-0991-e063-6394a90aae192024-04-08Warnings, Adverse reactionsExact identifier
application number: ANDA076943
rxcui: 198371
unii: W31X2H97FB
Clear Eyes Natural TearsPOLYVINYL ALCOHOL AND POVIDONEPrestige Brands Holdings, Inc.efba3eb0-798d-4635-b19b-4970e45b3cc92024-04-01WarningsExact identifier
unii: FZ989GH94E
REFRESH CLASSICPOLYVINYL ALCOHOL, POVIDONEA-S Medication Solutions3bf6193c-56db-45ad-844c-58eb8c33cba92024-03-14WarningsExact identifier
unii: FZ989GH94E
GOODSENSE ARTIFICIAL TEARSPOLYVINYL ALCOHOLProficient Rx LPf29c792c-6cb2-449f-b97d-6304a58dec2a2024-02-01WarningsExact identifier
unii: FZ989GH94E
GoodSense Artifical TearsPOLYVINYL ALCOHOL, AND POVIDONEProficient Rx LPcd24da78-fd90-4a9c-8e5f-f7fc56ec0fc92024-02-01WarningsExact identifier
unii: FZ989GH94E
TorsemideTORSEMIDEGolden State Medical Supply, Inc.a6055317-8826-df85-e053-2a95a90a53782023-12-28Warnings, Adverse reactionsExact identifier
application number: ANDA076943
rxcui: 198371
unii: W31X2H97FB
Sunmark Eye Drops Advanced Moisturizer/LubricantDEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINEStrategic Sourcing Services LLC0daa4e39-0447-44b6-a7d7-370b12bf94512023-12-23WarningsExact identifier
unii: FZ989GH94E
Meijer Artificial TearsPOLYVINYL ALCOHOL, POVIDONEMeijer Distribution, Inc.9feb3eec-a36f-8fc7-e053-2a95a90adcd32023-12-22WarningsExact identifier
unii: FZ989GH94E
Meijer Advanced Redness and Irritation ReliefDEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCIMeijer Distribution, Inc.9fea6d7a-a2cd-d26e-e053-2995a90a15f82023-12-22WarningsExact identifier
unii: FZ989GH94E
Walgreens Eye Drops Advanced Relief 15mLDEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCIWalgreen Company949f5560-fba7-2da8-e053-2995a90a23c22023-12-20WarningsExact identifier
unii: FZ989GH94E
Signature Care Eye Drops Advanced ReliefDEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCLBetter Living Brands LLC5d7228ce-f108-4cc2-9aec-8b4548c3a1552023-12-20WarningsExact identifier
unii: FZ989GH94E
Kroger Eye Drops Advanced ReliefDEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDEKroger Companyf7ad77fc-d890-25b9-e053-6394a90a2b122023-12-20WarningsExact identifier
unii: FZ989GH94E

Reported adverse events (FAERS/openFDA)#

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