FDA.reportPublic FDA data

NDC 57451-5024 - Hydrochlorothiazide

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
57451-5024
Package NDCs from labels
57451-5024-1, 57451-5024-2, 57451-5024-3
Manufacturer
Ipca Laboratories Limited
Effective date
2009-04-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Hydrochlorothiazide - Ipca Laboratories LimitedIpca Laboratories Limited2009-04-15HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57451-5024-1Hydrochlorothiazide30 in 1 BOTTLECAPSULE301
57451-5024-2Hydrochlorothiazide100 in 1 BOTTLECAPSULE1001
57451-5024-3Hydrochlorothiazide1000 in 1 BOTTLECAPSULE10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57451-5024HYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]13 package rows20090623_0bbc6889-0fd5-4763-97f4-061f5a50c7b1.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
HydrochlorothiazideACTIVE INGREDIENT0J48LPH2THHYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]1
HydrochlorothiazideACTIVE MOIETY0J48LPH2THHYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]1
black iron oxideINACTIVE INGREDIENTXM0M87F357HYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]1
colloidal silicon dioxideINACTIVE INGREDIENTETJ7Z6XBU4HYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]1
corn starchINACTIVE INGREDIENTO8232NY3SJHYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]1
D&C Red no. 28INACTIVE INGREDIENTHYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]1
D&C Yellow no. 10INACTIVE INGREDIENTHYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]1
FD&C Blue no.1INACTIVE INGREDIENTHYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]1
gelatinINACTIVE INGREDIENT2G86QN327LHYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]1
lactose monohydrateINACTIVE INGREDIENTEWQ57Q8I5XHYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]1
magnesium stearateINACTIVE INGREDIENT70097M6I30HYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]1
sodium lauryl sulfateINACTIVE INGREDIENT368GB5141JHYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]1
sodium starch glycolateINACTIVE INGREDIENTHYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]1
titanium dioxideINACTIVE INGREDIENT15FIX9V2JPHYDROCHLOROTHIAZIDE CAPSULE [IPCA LABORATORIES LIMITED]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 2 · 34 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HydrochlorothiazideHYDROCHLOROTHIAZIDEREMEDYREPACK INC.0789baef-3424-43ab-a3fb-4908172da5652026-07-24Warnings, Adverse reactionsExact identifier
rxcui: 199903
HydrochlorothiazideHYDROCHLOROTHIAZIDEPD-Rx Pharmaceuticals, Inc.cb7b7315-0170-492c-803f-60a6e75e55da2026-07-08Warnings, Adverse reactionsExact identifier
rxcui: 199903
HydrochlorothiazideHYDROCHLOROTHIAZIDEBryant Ranch Prepack2b21f3fc-4164-401a-803e-b982dea97e192026-05-14Warnings, Adverse reactionsExact identifier
rxcui: 199903
HydrochlorothiazideHYDROCHLOROTHIAZIDEPreferred Pharmaceuticals, Inc.918391e3-e8b3-4ceb-b4e7-c7c9617ea8822026-05-11Warnings, Adverse reactionsExact identifier
rxcui: 199903
HydrochlorothiazideHYDROCHLOROTHIAZIDEBryant Ranch Prepackff557069-f177-4e2e-91f4-675a033e27392026-04-14Warnings, Adverse reactionsExact identifier
rxcui: 199903
HydrochlorothiazideHYDROCHLOROTHIAZIDEBryant Ranch Prepack45316037-52ec-438f-8780-b2e983fef3f52026-03-31Warnings, Adverse reactionsExact identifier
rxcui: 199903
HydrochlorothiazideHYDROCHLOROTHIAZIDEScieGen Pharmaceuticals Inc911a18c1-120a-46b3-b7a8-25eb378434732026-02-10Warnings, Adverse reactionsExact identifier
rxcui: 199903
HydrochlorothiazideHYDROCHLOROTHIAZIDEAvPAKef56450d-86d3-2654-e053-2995a90a142c2026-01-08Warnings, Adverse reactionsExact identifier
rxcui: 199903
HydrochlorothiazideHYDROCHLOROTHIAZIDENorthwind Health Company, LLCf32ce8fe-6cbc-8a15-e053-2995a90a8eec2026-01-01Warnings, Adverse reactionsExact identifier
rxcui: 199903
hydrochlorothiazideHYDROCHLOROTHIAZIDENorthwind Health Company, LLCe3afa83d-c79c-848a-e053-2a95a90ac9222026-01-01Warnings, Adverse reactionsExact identifier
rxcui: 199903
hydrochlorothiazideHYDROCHLOROTHIAZIDEQPharma Inc578f74ea-53d1-4c44-b872-66033292abe02025-12-05Warnings, Adverse reactionsExact identifier
rxcui: 199903
HydrochlorothiazideHYDROCHLOROTHIAZIDEQPharma, Inc.5bacc909-6b02-4815-85ef-55fd25b1b1f72025-12-05Warnings, Adverse reactionsExact identifier
rxcui: 199903
hydrochlorothiazideHYDROCHLOROTHIAZIDEAmerican Health Packaging13ed002f-c5bb-401c-891a-70b70cbd8fb62025-06-18Warnings, Adverse reactionsExact identifier
rxcui: 199903
HydrochlorothiazideHYDROCHLOROTHIAZIDEA-S Medication Solutions02a481cb-ad80-41bb-82d3-c237b00ed8d72025-05-15Warnings, Adverse reactionsExact identifier
rxcui: 199903
HydrochlorothiazideHYDROCHLOROTHIAZIDEPreferred Pharmaceuticals Inc.82ad0fdf-5d47-4c2d-883b-f28b2d3fb6b02025-04-29Warnings, Adverse reactionsExact identifier
rxcui: 199903
hydrochlorothiazideHYDROCHLOROTHIAZIDEQuality Care Products LLCa2de8e26-ef5a-41c7-888b-990629b111452024-12-19Warnings, Adverse reactionsExact identifier
rxcui: 199903
HydrochlorothiazideHYDROCHLOROTHIAZIDEBryant Ranch Prepack8242c1de-f482-4a85-b977-610e71fa49042024-10-07Warnings, Adverse reactionsExact identifier
rxcui: 199903
HydrochlorothiazideHYDROCHLOROTHIAZIDERising Pharma Holdings, Inc.33f9c3ae-108d-469e-af6c-8be3b0f831392024-09-13Warnings, Adverse reactionsExact identifier
rxcui: 199903
HydrochlorothiazideHYDROCHLOROTHIAZIDEAurobindo Pharma Limitede31bd548-29ae-419a-831a-80ebb26e042f2024-06-26Warnings, Adverse reactionsExact identifier
rxcui: 199903
hydrochlorothiazideHYDROCHLOROTHIAZIDEBryant Ranch Prepack6a11a458-dc69-40ba-a58a-649733e0e8ab2024-05-29Warnings, Adverse reactionsExact identifier
rxcui: 199903

Reported adverse events (FAERS/openFDA)#

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