NDC 80425-0106-01 - 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: 80425-0106
Requested NDC: 80425-0106-01
Package NDCs from labels: 80425-0106-1, 80425-0106-01
Manufacturer: Advanced Rx Pharmacy of Tennessee, LLC
Effective date: 2024-12-31
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Prednisone - Advanced Rx Pharmacy of Tennessee, LLC	Advanced Rx Pharmacy of Tennessee, LLC	2024-12-31	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80425-0106-1	Prednisone	21 in 1 BOTTLE	TABLET	21		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80425-0106	PREDNISONE TABLET [ADVANCED RX PHARMACY OF TENNESSEE, LLC]	5	Current NDC, Legacy NDC, 1 package rows	20250101_b3dbf833-b929-8c85-e053-2995a90a5896.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
80425-0106-1	EA - Each	80425-0106	8ed41d10-5b10-42eb-aa9a-8926a007ea77	1	2023-06-06

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 13 of 13 · 242 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Prednisone	PREDNISONE	Proficient Rx LP	7a92b171-52ca-4948-81fc-e9a30597c5d8	2019-10-01	Warnings, Adverse reactions	Exact identifier unii: VB0R961HZT
Prednisone	PREDNISONE	Aphena Pharma Solutions - Tennessee, LLC	b902ed21-c776-4046-8fbc-9ce95b16b139	2017-12-21	Warnings, Adverse reactions	Exact identifier rxcui: 312617 unii: VB0R961HZT

Reported adverse events (FAERS/openFDA)#

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