NDC 70518-4191-01 - 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: 70518-4191
Requested NDC: 70518-4191-01
Package NDCs from labels: 70518-4191-0, 70518-4191-1, 70518-4191-2, 70518-4191-3, 70518-4191-4, 70518-4191-01
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-08-31
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
PredniSONE Tablets, USP	REMEDYREPACK INC.	2026-08-31	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
70518-4191-0	PredniSONE	14 in 1 BOTTLE, PLASTIC	TABLET	14	6
70518-4191-1	PredniSONE	30 in 1 BOTTLE, PLASTIC	TABLET	30	6
70518-4191-2	PredniSONE	20 in 1 BOTTLE, PLASTIC	TABLET	20	6
70518-4191-3	PredniSONE	10 in 1 BOTTLE, PLASTIC	TABLET	10	6
70518-4191-4	PredniSONE	18 in 1 BOTTLE, PLASTIC	TABLET	18	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70518-4191	PREDNISONE TABLET [REMEDYREPACK INC.]	4	Current NDC, 5 package rows	20250418_94715919-70bd-46c9-95fc-e151adf39cf9.zip

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 · 248 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Prednisone	PREDNISONE	Proficient Rx LP	35f504c3-1cf5-455d-8226-9ffeea606623	2022-05-01	Warnings, Adverse reactions	Exact identifier unii: VB0R961HZT
Prednisone	PREDNISONE	Proficient Rx LP	016d65c3-fff2-4e0c-9025-e2083cfa6a1f	2022-04-01	Warnings, Adverse reactions	Exact identifier rxcui: 312615 unii: VB0R961HZT
Prednisone	PREDNISONE	Proficient Rx LP	7d52bf53-76e3-4826-a12b-b16a8560bafc	2021-05-01	Warnings, Adverse reactions	Exact identifier rxcui: 198145 rxcui: 312617 unii: VB0R961HZT
Prednisone	PREDNISONE	Asclemed USA, Inc.	dc663fd3-b149-48ae-a3f3-6abaa4808cc6	2020-08-28	Warnings, Adverse reactions	Exact identifier rxcui: 198145 rxcui: 312615 rxcui: 312617 unii: VB0R961HZT
Prednisone	PREDNISONE	Proficient Rx LP	e4555299-af68-416f-8999-9bb703a45e77	2019-10-01	Warnings, Adverse reactions	Exact identifier rxcui: 312615 unii: VB0R961HZT
Prednisone	PREDNISONE	Proficient Rx LP	7c650dc8-43f6-4257-81ed-c93b00202d06	2019-10-01	Warnings, Adverse reactions	Exact identifier rxcui: 312617 unii: VB0R961HZT
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.