NDC11 68682070690

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
68682-0706-90	68682-0706
68682-706-90	68682-706

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
Diltiazem Hydrochloride	DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE TABLETS	Oceanside Pharmaceuticals	73b3607a-99d0-44d8-92ef-0074684c9d7d	2025-04-01	Warnings, Adverse reactions	Exact identifier ndc (package): 68682-706-90 ndc (product): 68682-706 ndc11 (package): 68682070690

Reported adverse events (FAERS/openFDA)#

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