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 10 of 13 · 256 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PrednisonePREDNISONEAdvanced Rx of Tennessee, LLCaf861c38-3293-13fe-e053-2995a90a99322024-12-31Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PrednisonePREDNISONEAdvanced Rx Pharmacy of Tennessee, LLCb3dbf833-b929-8c85-e053-2995a90a58962024-12-31Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PrednisonePREDNISONEAdvanced Rx Pharmacy of Tennessee, LLCe1e7d14b-80b2-f57e-e053-2995a90af1122024-12-31Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
PrednisonePREDNISONEAdvanced Rx Pharmacy of Tennessee, LLCb3dbff9f-610f-7782-e053-2a95a90a71c12024-12-31Warnings, Adverse reactionsExact identifier
rxcui: 312615
unii: VB0R961HZT
Household AntigensACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, BUTYL ACETATE, ETHYL ACETATE, TOLUENE, XYLENE, BISPHENOL A, PETROLEUM, FORMALINUM, GLYPHOSATE, METHYLPARABEN, NAPHTHALINUM, PROPYLPARABEN, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUR, PARAFFINUMEnergique, Inc.f3db63df-62a4-48d6-92e7-94e4a57015522024-12-20WarningsExact identifier
unii: 368GB5141J
PREDNISONEPREDNISONENuCare Pharmaceuticals, Inc.28f2733e-963e-f0e0-e063-6394a90a0a9d2024-12-10Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PrednisonePREDNISONENuCare Pharmaceuticals,Inc.1b42449a-2be8-e4fb-e063-6394a90aff982024-11-08Warnings, Adverse reactionsExact identifier
application number: ANDA211575
rxcui: 312615
unii: VB0R961HZT
PREDNISONEPREDNISONEA-S Medication Solutions3bfdc4d7-ba8e-422a-96e3-3c3ba587eab12024-11-08Warnings, Adverse reactionsExact identifier
rxcui: 198148
unii: VB0R961HZT
PrednisonePREDNISONEDirect_Rx26194836-90c9-6909-e063-6294a90a6f982024-11-04Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
prednisonePREDNISONEA-S Medication Solutions81cef50e-394a-49b3-8723-28df68a742d62024-10-22Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
prednisonePREDNISONEA-S Medication Solutionsaaea2307-7893-48e9-af64-26172d08d4e82024-10-22Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
Household AntigensACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, BUTYL ACETATE, ETHYL ACETATE, TOLUENE, XYLENE, BISPHENOL A, PETROLEUM, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUREnergique, Inc.87c92497-8a51-4977-87fe-e0b4c6bafb192024-09-27WarningsExact identifier
unii: 368GB5141J
prednisonePREDNISONEA-S Medication Solutionsd40a97f6-60d1-4dbc-b4dc-650d82af5fae2024-08-30Warnings, Adverse reactionsExact identifier
rxcui: 198146
unii: VB0R961HZT
prednisonePREDNISONEA-S Medication Solutions90b8b43e-01f9-4503-91c4-2b3cbae91a832024-08-15Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
prednisonePREDNISONEA-S Medication Solutionsf4cc64f8-781f-437a-a4a7-2d163026d1c22024-08-15Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
PrednisonePREDNISONENuCare Pharmaceuticals,Inc.62fdf3c2-cfa9-d573-e053-2a91aa0a833b2024-08-14Warnings, Adverse reactionsExact identifier
rxcui: 312615
unii: VB0R961HZT
PrednisonePREDNISONENuCare Pharmaceuticals,Inc.62ec965c-e682-9920-e053-2a91aa0adcdb2024-08-14Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
PrednisonePREDNISONEBryant Ranch Prepack91167f27-6f36-4b89-a530-be26209e43012024-08-14Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
prednisonePREDNISONENCS HealthCare of KY, LLC dba Vangard Labs7b60255f-7d0b-4f91-a75c-6682ac446f6b2024-08-12Warnings, Adverse reactionsExact identifier
rxcui: 198145
rxcui: 312615
unii: VB0R961HZT
prednisonePREDNISONEBryant Ranch Prepack4433a882-ff79-4a9d-8db8-1977c5cd04cf2024-08-08Warnings, Adverse reactionsExact identifier
rxcui: 312615
unii: VB0R961HZT

Reported adverse events (FAERS/openFDA)#

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