NDC 70518-4524-01 - Prednisolone Sodium Phosphate

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
70518-4524
Requested NDC
70518-4524-01
Package NDCs from labels
70518-4524-1, 70518-4524-0, 70518-4524-3, 70518-4524-2, 70518-4524-5, 70518-4524-4, 70518-4524-01
Manufacturer
REMEDYREPACK INC.
Effective date
2026-02-10
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PREDNISOLONE SODIUM PHOSPHATE ORAL SOLUTION (15 mg Prednisolone Base per 5 mL)REMEDYREPACK INC.2026-02-10HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-4524-0Prednisolone Sodium Phosphate2 in 1 BOXSOLUTION23
70518-4524-1Prednisolone Sodium Phosphate25 mL in 1 CUPSOLUTION253
70518-4524-2Prednisolone Sodium Phosphate5 in 1 BOXSOLUTION53
70518-4524-3Prednisolone Sodium Phosphate10 mL in 1 CUPSOLUTION103
70518-4524-4Prednisolone Sodium Phosphate10 in 1 BOXSOLUTION103
70518-4524-5Prednisolone Sodium Phosphate5 mL in 1 CUPSOLUTION53

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 37 of 37 · 723 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CerebroforceCAPSICUM ANNUUM, GINKGO BILOBA, GELSEMIUM SEMPERVIRENS, KALI PHOSPHORICUM, LYCOPODIUM CLAVATUM, PHOSPHORUS, ARSENICUM ALBUMBioActive Nutritional, Incf998ed3f-56a5-4497-be5b-9a819fe8be692016-07-13WarningsExact identifier
unii: CI71S98N1Z
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
TIS-U-SOLSODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATEBaxter Healthcare Corporation9da4121f-d62d-4da4-8dfb-0494da16015f2014-02-21Exact identifier
unii: 4J9FJ0HL51

Reported adverse events (FAERS/openFDA)#

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