FDA.reportPublic FDA data

NDC 81033-043 - amiloride hydrochloride

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
81033-043
Package NDCs from labels
81033-043-11
Manufacturer
Kesin Pharma Corporation
Effective date
2026-11-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
amiloride hydrochloride - Kesin Pharma CorporationKesin Pharma Corporation2026-11-11HUMAN PRESCRIPTION DRUG LABEL

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 2 of 2 · 30 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dementia Drops 2117DEMENTIA DROPSProfessional Complementary Health Formulas83aec02b-bc62-49a2-ba35-4ac94f9bfc6e2026-01-08WarningsExact identifier
unii: L11K75P92J
Medicated Cornstarch Baby PowderACTIVE CORN STARCHDavion, Inc.e39032d1-c8cd-4a41-af10-126970b8ad382025-12-29WarningsExact identifier
unii: O8232NY3SJ
Schuessler Tissue Salts Calc Phos Bone Health 2CALCAREA PHOSPHORICAMartin & Pleasance Pty Ltdc277f1d8-2ee0-4111-adb6-38998f77dede2025-07-18WarningsExact identifier
unii: L11K75P92J
Schuessler Tissue Salts Calc Phos Bone Health 2CALCAREA PHOSPHORICAMartin & Pleasance Pty Ltd81d59754-1b36-4f71-aec1-5335b003a96f2025-07-01WarningsExact identifier
unii: L11K75P92J
Pure Cornstarch BabyCORN STARCHWalgreen Companyd0e9bd13-b568-4f7e-b036-8d23e71ad8bf2024-03-25WarningsExact identifier
unii: O8232NY3SJ
amiloride hydrochlorideAMILORIDE HYDROCHLORIDEPadagis US LLC2b70cf0c-45be-428f-b396-5001ed4e30fc2023-05-05Boxed warning, Warnings, Adverse reactionsExact identifier
application number: NDA018200
ndc (product): 0574-0292
rxcui: 977880
spl id: 416c3aaf-7390-40cf-995a-31258156b4f2
spl set id: 2b70cf0c-45be-428f-b396-5001ed4e30fc
unii: FZJ37245UC
Amiloride HydrochlorideAMILORIDE HYDROCHLORIDESigmapharm Laboratories, LLCde12b6f3-3791-4d78-90e6-c487cf9517382023-01-10Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 977880
Amiloride Hydrochloride and HydrochlorothiazideAMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDETeva Pharmaceuticals USA, Inc.8b2c581a-f955-4a8e-bf85-e768e903fd102022-12-27Boxed warning, Warnings, Adverse reactionsExact identifier
unii: FZJ37245UC
Melange combinationCALCAREA SULPHURICA, CALCIUM PHOSPHORICUM, KALI MURIATICUM, KALIUM PHOSPHORICUM, KALI SULPHURICUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRIUM SULFURICUM, CALCAREA FLUORICA, FERRUM PHOSPHORICUM, SILICEASeroyal USA0a071fbf-0075-4479-e054-00144ff8d46c2021-07-14WarningsExact identifier
unii: L11K75P92J
MEDULLOSSEINUM PLEXARNICA MONTANA, CALCAREA PHOSPHORICA, CALENDULA OFFICINALIS, HYPERICUM PERFORATUM, MEDULLOSSEINUM, PULSATILLA, RUTA GRAVEOLENS, SYMPHYTUM OFFICINALESeroyal USA22b7eafe-ef76-0677-e054-00144ff88e882020-10-09WarningsExact identifier
unii: L11K75P92J

Reported adverse events (FAERS/openFDA)#

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