NDC11 00338966901

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
00338-9669-01	00338-9669
00338-9669-1	00338-9669
0338-9669-01	0338-9669

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
ANTICOAGULANT SODIUM CITRATE	TRISODIUM CITRATE DIHYDRATE	Baxter Healthcare Corporation	7025a0f9-1a56-4416-a3a4-925d755aed90	2024-04-02		Exact identifier ndc (package): 0338-9669-01 ndc (product): 0338-9669 ndc11 (package): 00338966901

Reported adverse events (FAERS/openFDA)#

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