NDC11 63323037700

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
63323-0377-0	63323-0377
63323-0377-00	63323-0377
63323-377-00	63323-377

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Octreotide	OCTREOTIDE ACETATE	Fresenius Kabi USA, LLC	d6a9a800-889d-417f-b533-1913197d0022	2024-05-23	Warnings, Adverse reactions	Exact identifier ndc (product): 63323-377
Octreotide	OCTREOTIDE ACETATE	Fresenius Kabi USA, LLC	f278f0d8-4062-420a-97c3-3a8b88253a08	2024-05-07	Warnings, Adverse reactions	Exact identifier ndc (package): 63323-377-00 ndc (product): 63323-377 ndc11 (package): 63323037700

Reported adverse events (FAERS/openFDA)#

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