NDC11 70069005101

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
70069-0051-01	70069-0051
70069-0051-1	70069-0051
70069-051-01	70069-051

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
DORZOLAMIDE HYDROCHLORIDE and TIMOLOL MALEATE	DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE	Somerset Therapeutics, LLC	17f04726-725f-4839-911d-47fc5e02baae	2024-09-18	Warnings, Adverse reactions	Exact identifier ndc (package): 70069-051-01 ndc (product): 70069-051 ndc11 (package): 70069005101

Reported adverse events (FAERS/openFDA)#

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