NDC11 70710136703

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
70710-1367-03	70710-1367
70710-1367-3	70710-1367

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
Emtricitabine and tenofovir disoproxil fumarate	EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE	Zydus Pharmaceuticals USA Inc.	7def7a95-e69e-4985-974a-efacadcecc95	2024-05-10	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 70710-1367-3 ndc (product): 70710-1367 ndc11 (package): 70710136703

Reported adverse events (FAERS/openFDA)#

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