NDC 51662-1263-2 - SOLU-MEDROL

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: 51662-1263
Requested NDC: 51662-1263-2
Package NDCs from labels: 51662-1263-1, 51662-1263-2, 51662-1263-3
Manufacturer: HF Acquisition Co. LLC, DBA HealthFirst
Effective date: 2024-01-29
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
SOLU-MEDROL - HF Acquisition Co. LLC, DBA HealthFirst	HF Acquisition Co. LLC, DBA HealthFirst	2024-01-29	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51662-1263-1	2020-02-07	C162847	48780-1	9d75b9d0-90a6-f424-e053-dadaa90a57ce	SOLU-MEDROL® 125MG PER VIAL 2mL ACT-O-VIAL®
51662-1263-1	2020-01-31	C162847	48780-1	9d75b9d0-90a6-f424-e053-dadaa90a57ce	SOLU-MEDROL® 125MG PER VIAL 2mL ACT-O-VIAL®

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
51662-1263-1	SOLU-MEDROL	1 mL in 1 VIAL, SINGLE-USE	INJECTION, POWDER, FOR SOLUTION	1	7
51662-1263-2	SOLU-MEDROL	1 mL in 1 POUCH	INJECTION, POWDER, FOR SOLUTION	1	7
51662-1263-3	SOLU-MEDROL	25 in 1 CASE	INJECTION, POWDER, FOR SOLUTION	25	7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51662-1263	SOLU-MEDROL INJECTION, POWDER, FOR SOLUTION [HF ACQUISITION CO. LLC, DBA HEALTHFIRST]	7	Current NDC, Legacy NDC, 3 package rows	20240131_74e448ed-f4b4-8d09-e053-2991aa0a7500.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 4 of 4 · 66 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
InterSol	PLATELET ADDITIVE 3	Fenwal, Inc.	a00c4a93-cde2-4753-81f7-0d6fee9fb690	2020-10-20	Warnings, Adverse reactions	Exact identifier unii: GR686LBA74
FREDS SALINE TWIN PACK LAXATIVE	SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM	FRED'S	7d15057f-eb3b-477f-ab14-68c3c38ea910	2018-12-26	Warnings	Exact identifier unii: GR686LBA74
Marcs Twin Pack	SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM	Marc Glassman Inc.	66348ee5-803a-4b78-94dd-55bc9d3543c3	2018-07-10	Warnings	Exact identifier unii: GR686LBA74
QUALITY CHOICE SINGLE SALINE LAXATIVE	SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM	Alcyon Health, LLC.	eb499c7f-9c7b-4097-83a3-82aabffd6beb	2017-07-12	Warnings	Exact identifier unii: GR686LBA74
Pro-Enema Single Saline Laxative	SODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM	Propharma Medical Supplies	e53c5eda-21da-4aed-a592-315100167cc2	2017-06-08	Warnings	Exact identifier unii: GR686LBA74
Saline Laxative Cherry Laxative	SODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM	Dolgencorp Inc.	ca3c00d9-4301-4de8-94f5-34f1bcc761ab	2017-04-13	Warnings	Exact identifier unii: GR686LBA74

Reported adverse events (FAERS/openFDA)#

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