FDA.reportPublic FDA data

NDC 80425-0486-01 - Prednisone

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
80425-0486
Requested NDC
80425-0486-01
Package NDCs from labels
80425-0486-1, 80425-0486-2, 80425-0486-3, 80425-0486-4, 80425-0486-5, 80425-0486-01
Manufacturer
Advanced Rx of Tennessee, LLC
Effective date
2025-04-04
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Prednisone - Advanced Rx of Tennessee, LLCAdvanced Rx of Tennessee, LLC2025-04-04HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80425-0486-1Prednisone21 in 1 BOTTLETABLET212
80425-0486-2Prednisone14 in 1 BOTTLETABLET142
80425-0486-3Prednisone10 in 1 BOTTLETABLET102
80425-0486-4Prednisone15 in 1 BOTTLETABLET152
80425-0486-5Prednisone20 in 1 BOTTLETABLET202

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80425-0486PREDNISONE TABLET [ADVANCED RX OF TENNESSEE, LLC]2Current NDC, 5 package rows20250410_30956dd5-fe19-d5a9-e063-6394a90a2549.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
80425-0486-1EA - Each80425-048614b47980-5e35-4c21-81e3-9783b105b21412025-05-14
80425-0486-2EA - Each80425-0486ec265645-937d-4699-9c0a-e0f5196c43c812025-05-14
80425-0486-3EA - Each80425-048656012a15-551c-4149-896d-54de13c6022712025-05-14
80425-0486-4EA - Each80425-0486c41b5398-3087-42d4-bbc9-1eb784ab9acc12025-05-14
80425-0486-5EA - Each80425-048652b341a3-b8aa-4964-bd16-6b9c29c8b88812025-05-14

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 12 of 13 · 256 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
prednisonePREDNISONEMedsource Pharmaceuticals131780a0-31f3-6588-e063-6294a90a2f8e2024-03-07Warnings, Adverse reactionsExact identifier
rxcui: 312615
unii: VB0R961HZT
PredniSONEPREDNISONENuCare Pharmaceuticals,Inc.1289c6d2-2707-baca-e063-6294a90a750d2024-02-29Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PrednisonePREDNISONEA-S Medication Solutions95cf05e5-1446-43f5-8447-c04877a747812024-02-27Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
PrednisonePREDNISONEANI Pharmaceuticals, Inc.7335a293-992b-490c-ab8a-66a7ca1eea302024-02-16Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PREDNISONEPREDNISONEAurobindo Pharma Limited7b33767f-a520-4470-8f3f-4e86b38d615a2024-02-16Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PREDNISONEPREDNISONEAurobindo Pharma Limitedb1ac4c92-e1fd-4015-b172-0932790ae0192024-02-16Warnings, Adverse reactionsExact identifier
rxcui: 198145
rxcui: 198146
rxcui: 312615
rxcui: 198148
rxcui: 312617
unii: VB0R961HZT
PrednisonePREDNISONENuCare Pharmaceuticals,Inc.63102d75-9b2b-84a9-e053-2a91aa0a317d2024-02-09Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PrednisonePREDNISONEA-S Medication Solutions410988ea-456a-454e-932c-fcbdbef04ba92024-01-18Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
PrednisonePREDNISONEA-S Medication Solutions44069d49-4cf4-4f1e-9fbd-b496c6ca81a12024-01-18Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
prednisonePREDNISONEA-S Medication Solutions17278e0a-cbff-4a95-96ee-f34f7466faa02023-11-24Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PrednisonePREDNISONEChartwell RX, LLC92483276-d55c-42c6-8bbc-27137ff252962023-09-06Warnings, Adverse reactionsExact identifier
rxcui: 312615
unii: VB0R961HZT
prednisonePREDNISONEProficient Rx LP6a0c1192-8ce4-466d-a0f3-d878d67349cf2023-09-01Warnings, Adverse reactionsExact identifier
rxcui: 312615
unii: VB0R961HZT
PrednisonePREDNISONEProficient Rx LP5961b1d4-6a4c-452f-b3f1-c99f3a9a64452023-09-01Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
PredniSONEPREDNISONEA-S Medication Solutions0060b86b-0b79-4c54-a7be-97683a933a052023-08-31Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PredniSONEPREDNISONEA-S Medication Solutionsf11c190e-edf8-454d-82c4-1ed769b5a6d22023-08-31Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PredniSONEPREDNISONEA-S Medication Solutions6f0719a2-1759-4354-9363-bb9fb3bddb3d2023-08-31Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
Household AntigensACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHURBioActive Nutritional3382df85-3ec5-4371-830e-4ed345b8f51b2023-07-14WarningsExact identifier
unii: 368GB5141J
PneumotoxTRITICUM AESTIVUM, ALFALFA, ARNICA MONTANA, ASCLEPIAS TUBEROSA, CHAMOMILLA, ECHINACEA (ANGUSTIFOLIA), EUCALYPTUS GLOBULUS, FUCUS VESICULOSUS, HORDEUM VULGARE, IODIUM, NASTURTIUM AQUATICUM, PLANTAGO MAJOR, RAPHANUS SATIVUS, TRIFOLIUM PRATENSE, TRIGONELLA FOENUM-GRAECUM, SYMPHYTUM OFFICINALE, LUNG (SUIS), ORYZA SATIVA, SILICEA, ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, ARSENICUM ALBUM, NATRUM MURIATICUM, NITRICUM ACIDUM,BioActive Nutritional, Inc.f8846fb1-92e5-4f8e-b3b3-bc620df90a622023-07-12WarningsExact identifier
unii: 368GB5141J
prednisonePREDNISONEProficient Rx LP6ec5b58c-65e9-47ee-b2ac-7d0b395a06302023-07-01Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
prednisonePREDNISONEProficient Rx LP22d9fd96-cad5-4762-9a56-0ff63357ed9e2023-02-01Warnings, Adverse reactionsExact identifier
rxcui: 198148
unii: VB0R961HZT

Reported adverse events (FAERS/openFDA)#

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