NDC11 00093550356

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
00093-5503-56	00093-5503
0093-5503-56	0093-5503

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
Olanzapine and Fluoxetine	OLANZAPINE AND FLUOXETINE	Teva Pharmaceuticals USA, Inc.	3c28cf18-01a3-468a-ab3e-8aa82f918251	2026-03-31	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 0093-5503-56 ndc (product): 0093-5503 ndc11 (package): 00093550356

Reported adverse events (FAERS/openFDA)#

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