NDC11 70436019301

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
70436-0193-01	70436-0193
70436-0193-1	70436-0193
70436-193-01	70436-193

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	Slate Run Pharmaceuticals, LLC	e66665e8-22eb-f5cd-e053-2a95a90a72e4	2026-08-05	Warnings, Adverse reactions	Exact identifier ndc (package): 70436-193-01 ndc (product): 70436-193 ndc11 (package): 70436019301

Reported adverse events (FAERS/openFDA)#

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