NDC11 00093324101

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
00093-3241-01	00093-3241
00093-3241-1	00093-3241
0093-3241-01	0093-3241

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
bisoprolol fumarate and hydrochlorothiazide	BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE	Teva Pharmaceuticals USA, Inc.	27d52b23-e3e2-4339-b00e-cd0fec43ffbb	2026-08-11	Warnings, Adverse reactions	Exact identifier ndc (package): 0093-3241-01 ndc (product): 0093-3241 ndc11 (package): 00093324101

Reported adverse events (FAERS/openFDA)#

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