NDC11 70404007716

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
70404-0077-16	70404-0077
70404-077-16	70404-077

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	PREDNISOLONE ORAL	Tulex Pharmaceuticals Inc	757b41c4-a0fe-4a09-8816-a4cdb7558f41	2026-07-08	Warnings, Adverse reactions	Exact identifier ndc (package): 70404-077-16 ndc (product): 70404-077 ndc11 (package): 70404007716

Reported adverse events (FAERS/openFDA)#

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