NDC 68071-3729-01 - 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: 68071-3729
Requested NDC: 68071-3729-01
Package NDCs from labels: 68071-3729-1, 68071-3729-2, 68071-3729-9, 68071-3729-5, 68071-3729-01
Manufacturer: NuCare Pharmaceuticals,Inc.
Effective date: 2025-06-20
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 Rx only	NuCare Pharmaceuticals,Inc.	2025-06-20	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
68071-3729-1	PREDNISONE	21 in 1 BOTTLE	TABLET	21	4
68071-3729-2	PREDNISONE	20 in 1 BOTTLE	TABLET	20	4
68071-3729-5	PREDNISONE	15 in 1 BOTTLE	TABLET	15	4
68071-3729-9	PREDNISONE	90 in 1 BOTTLE	TABLET	90	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68071-3729	PREDNISONE TABLET [NUCARE PHARMACEUTICALS,INC.]	3	Current NDC, 4 package rows	20250116_27d8dcad-a024-ed85-e063-6394a90a420d.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 · 246 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
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.