NDC11 70756031531

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
70756-0315-31	70756-0315
70756-315-31	70756-315

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
telmisartan and hydrochlorothiazide	TELMISARTAN AND HYDROCHLOROTHIAZIDE	Lifestar Pharma LLC	0c1bd0f4-034e-486c-ae46-2855c8c9ebda	2025-08-20	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 70756-315-31 ndc (product): 70756-315 ndc11 (package): 70756031531

Reported adverse events (FAERS/openFDA)#

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