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 9 of 13 · 256 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PrednisonePREDNISONEBryant Ranch Prepack0b2c2085-c4da-4441-ae5e-eefe26fd199e2025-04-25Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PredniSONEPREDNISONEHikma Pharmaceuticals USA Inc.263ed4fa-3c29-4abb-9cb1-bc016bd34a052025-04-22Warnings, Adverse reactionsExact identifier
rxcui: 198145
rxcui: 312615
rxcui: 312617
unii: VB0R961HZT
PredniSONEPREDNISONEHikma Pharmaceuticals USA Inc.3115aef0-fd50-4ec8-a064-3effb695f3f22025-04-22Warnings, Adverse reactionsExact identifier
rxcui: 198145
rxcui: 198146
rxcui: 312615
rxcui: 198148
rxcui: 312617
unii: VB0R961HZT
prednisonePREDNISONEAdvanced Rx of Tennessee, LLC2d0562ad-6175-833c-e063-6394a90ad0292025-04-04Warnings, Adverse reactionsExact identifier
rxcui: 198145
rxcui: 312615
rxcui: 312617
unii: VB0R961HZT
PrednisonePREDNISONEAdvanced Rx of Tennessee, LLC30956dd5-fe19-d5a9-e063-6394a90a25492025-04-04Warnings, Adverse reactionsExact identifier
application number: ANDA211575
ndc (package): 80425-0486-2
ndc (package): 80425-0486-5
ndc (package): 80425-0486-3
ndc (package): 80425-0486-1
ndc (package): 80425-0486-4
ndc (product): 80425-0486
ndc11 (package): 80425048601
rxcui: 312615
spl id: 31fa1bbe-5072-482a-e063-6394a90aff74
spl set id: 30956dd5-fe19-d5a9-e063-6394a90a2549
unii: VB0R961HZT
PrednisonePREDNISONENuCare Pharmaceuticals, Inc.31cfc21f-726b-ae80-e063-6294a90a9af42025-04-02Warnings, Adverse reactionsExact identifier
application number: ANDA211575
rxcui: 198145
unii: VB0R961HZT
prednisonePREDNISONEProficient Rx LPc2f477da-0b99-4fc4-89ca-94831de950a32025-04-01Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
prednisonePREDNISONEBryant Ranch Prepack9a2d3bee-610b-44dc-8266-869aaf08f0d12025-03-27Warnings, Adverse reactionsExact identifier
rxcui: 312615
unii: VB0R961HZT
PrednisonePREDNISONEAdvanced Rx of Tennessee, LLC309580a7-c3bb-e53b-e063-6394a90a15632025-03-17Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
YVTYVT MICRODERMABRASION FACIAL SCRUBYVTYVT MICRODERMABRASION FACIAL SCRUBBeijing JUNGE Technology Co., Ltd.2f30fc45-42e2-c766-e063-6394a90a8d682025-02-28WarningsExact identifier
unii: OP1R32D61U
prednisonePREDNISONEBryant Ranch Prepackf0354431-4968-4e34-969b-6985d73700a42025-02-25Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
prednisonePREDNISONEA-S Medication Solutions1cb252f0-fd01-4620-bf88-2108fc1ea6152025-02-19Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PrednisonePREDNISONEGolden State Medical Supply, Inc.1e05e071-0407-0970-e063-6294a90a6c652025-02-18Warnings, Adverse reactionsExact identifier
rxcui: 198145
rxcui: 312615
rxcui: 312617
unii: VB0R961HZT
PredniSONEPREDNISONEAdvanced Rx of Tennessee, LLC2e62cf2e-dcbe-c15e-e063-6294a90a81682025-02-17Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PREDNISONEPREDNISONEAdvanced Rx of Tennessee, LLC2e62cf2e-dcbf-c15e-e063-6294a90a81682025-02-17Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PredniSONEPREDNISONEAdvanced Rx of Tennessee, LLC2e630aa1-eccd-f5eb-e063-6294a90a47452025-02-17Warnings, Adverse reactionsExact identifier
rxcui: 198145
rxcui: 312617
unii: VB0R961HZT
PrednisonePREDNISONECoupler LLC2d99223a-853a-7640-e063-6394a90a260a2025-02-07Warnings, Adverse reactionsExact identifier
rxcui: 198146
unii: VB0R961HZT
PREDNISONEPREDNISONEPreferred Pharmaceuticals Inc.94d82acb-ff31-492f-bd51-b23e15d881d62025-01-23Warnings, Adverse reactionsExact identifier
rxcui: 312615
unii: VB0R961HZT
PrednisonePREDNISONEDirect_Rxfd8eb82e-52df-c368-e053-6294a90ac6b02025-01-22Warnings, Adverse reactionsExact identifier
rxcui: 198148
unii: VB0R961HZT
PrednisonePREDNISONEAdvanced Rx of Tennessee, LLCaf863b9e-964b-3b1e-e053-2995a90ab93a2024-12-31Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT

Reported adverse events (FAERS/openFDA)#

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