NDC11 00310320004

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
00310-3200-04	00310-3200
00310-3200-4	00310-3200
0310-3200-04	0310-3200

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
ANDEXXA	ANDEXANET ALFA	AstraZeneca Pharmaceuticals LP	2d9d90a6-63e6-46ef-96ff-dd6519ae7b6c	2025-05-23	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 0310-3200-04 ndc (product): 0310-3200 ndc11 (package): 00310320004

Reported adverse events (FAERS/openFDA)#

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