NDC11 00093240101

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
00093-2401-01	00093-2401
00093-2401-1	00093-2401
0093-2401-01	0093-2401

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
Hydroxychloroquine Sulfate	HYDROXYCHLOROQUINE SULFATE	Teva Pharmaceuticals USA, Inc.	5f3e49b2-dc11-40a9-b366-c88e36a471e5	2024-02-29	Warnings, Adverse reactions	Exact identifier ndc (package): 0093-2401-01 ndc (product): 0093-2401 ndc11 (package): 00093240101

Reported adverse events (FAERS/openFDA)#

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