NDC11 81033002105

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
81033-0021-05	81033-0021
81033-0021-5	81033-0021
81033-021-05	81033-021

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
prednisoLONE sodium phosphate	PREDNISOLONE SODIUM PHOSPHATE	Kesin Pharma	4c0dcbfd-2848-9bd0-e063-6394a90af5a7	2026-03-27	Warnings, Adverse reactions	Exact identifier ndc (package): 81033-021-05 ndc (product): 81033-021 ndc11 (package): 81033002105

Reported adverse events (FAERS/openFDA)#

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