NDC11 79481015201

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
79481-0152-01	79481-0152
79481-0152-1	79481-0152
79481-152-01	79481-152

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
DUAL ACTION BACK PAIN RELIEVER	ACETAMINOPHEN, IBUPROFEN	Meijer, Inc.	8d9a0c56-ef22-45a6-8b1d-d2b2f3247210	2026-03-19	Warnings	Exact identifier ndc (package): 79481-0152-1 ndc (product): 79481-0152 ndc11 (package): 79481015201

Reported adverse events (FAERS/openFDA)#

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