FDA.reportPublic FDA data

NDC 50989-286-52 - PrednisTab

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
50989-286
Requested NDC
50989-286-52
Package NDCs from labels
50989-286-52
Manufacturer
Vedco Inc. | LLOYD, Inc. of Iowa
Effective date
2024-10-17
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PrednisTab - Vedco Inc. | LLOYD, Inc. of IowaVedco Inc. | LLOYD, Inc. of Iowa2024-10-17PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50989-286-52PrednisTab500 in 1 BOTTLE, PLASTICTABLET5009

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50989-286PREDNISTAB (PREDNISOLONE) TABLET [VEDCO INC.]91 package rows20241020_5fdc36eb-3bb8-4877-81d5-112d3ddf8573.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PREDNISOLONEACTIVE INGREDIENT9PHQ9Y1OLMPREDNISTAB (PREDNISOLONE) TABLET [VEDCO INC.]2
PREDNISOLONEACTIVE MOIETY9PHQ9Y1OLMPREDNISTAB (PREDNISOLONE) TABLET [VEDCO INC.]2
.ALPHA.-TOCOPHEROLINACTIVE INGREDIENTH4N855PNZ1PREDNISTAB (PREDNISOLONE) TABLET [VEDCO INC.]2
ANHYDROUS CITRIC ACIDINACTIVE INGREDIENTXF417D3PSLPREDNISTAB (PREDNISOLONE) TABLET [VEDCO INC.]2
BUTYLATED HYDROXYTOLUENEINACTIVE INGREDIENT1P9D0Z171KPREDNISTAB (PREDNISOLONE) TABLET [VEDCO INC.]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UPREDNISTAB (PREDNISOLONE) TABLET [VEDCO INC.]2
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XPREDNISTAB (PREDNISOLONE) TABLET [VEDCO INC.]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30PREDNISTAB (PREDNISOLONE) TABLET [VEDCO INC.]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJPREDNISTAB (PREDNISOLONE) TABLET [VEDCO INC.]2

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 1 ยท 12 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PrednisolonePREDNISOLONE ORALTRUPHARMA, LLC4f83514d-5342-4748-a0d3-b0306ca303c82026-09-02Warnings, Adverse reactionsExact identifier
unii: 9PHQ9Y1OLM
PrednisolonePREDNISOLONE ORALTulex Pharmaceuticals Inc757b41c4-a0fe-4a09-8816-a4cdb7558f412026-07-08Warnings, Adverse reactionsExact identifier
unii: 9PHQ9Y1OLM
PrednisolonePREDNISOLONEA-S Medication Solutions35f0b197-c3ae-445a-8da7-9ffcd4472e052026-01-23Warnings, Adverse reactionsExact identifier
unii: 9PHQ9Y1OLM
PREDNISOLONEPREDNISOLONEZhejiang Xianju Pharmaceutical Co., Ltd.52e6e21d-94b8-41a0-8d13-371c0e66bcee2026-01-05Warnings, Adverse reactionsExact identifier
rxcui: 198142
unii: 9PHQ9Y1OLM
PrednisolonePREDNISOLONE ORALChartwell Governmental & Specialty RX, LLC.2dac9898-6492-4f34-ad86-83a902e0fe0b2025-11-18Warnings, Adverse reactionsExact identifier
unii: 9PHQ9Y1OLM
PrednisolonePREDNISOLONE ORAL SOLUTIONHeritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.b079834f-9aa3-4db9-bd53-de28e8f81c042025-02-18Warnings, Adverse reactionsExact identifier
unii: 9PHQ9Y1OLM
PrednisolonePREDNISOLONEPAI Holdings, LLC dba PAI Pharmacebd7b5b-8e9f-4de9-9fcf-8ee0661fede32024-08-19Warnings, Adverse reactionsExact identifier
unii: 9PHQ9Y1OLM
PREDNISOLONEPREDNISOLONEHisun Pharmaceuticals USA, Inc.16d4e064-66d3-4497-8c7d-3aa355f91e1d2024-08-15Warnings, Adverse reactionsExact identifier
rxcui: 198142
unii: 9PHQ9Y1OLM
PrednisolonePREDNISOLONEChartwell RX, LLC2e965355-f7f2-4dd3-9c5c-1524c6f39c912024-06-17Warnings, Adverse reactionsExact identifier
rxcui: 198142
unii: 9PHQ9Y1OLM
PrednisolonePREDNISOLONE ORALChartwell RX, LLCaa40f582-cced-4e6e-90f0-10ab310ab2a72024-06-03Warnings, Adverse reactionsExact identifier
unii: 9PHQ9Y1OLM
PREDNISOLONEPREDNISOLONEAurobindo Pharma Limited070f1937-50a5-457f-bef5-4e597014e26d2024-02-16Warnings, Adverse reactionsExact identifier
rxcui: 198142
unii: 9PHQ9Y1OLM
PrednisoLONEPREDNISOLONELannett Company, Inc.86652e2d-664a-4388-a611-c2a9aa4a4bc82024-02-14Warnings, Adverse reactionsExact identifier
unii: 9PHQ9Y1OLM

Reported adverse events (FAERS/openFDA)#

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