NDC11 61480013705

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
61480-0137-05	61480-0137
61480-0137-5	61480-0137
61480-137-05	61480-137

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
Acunol	NICKEL SULFATE, POTASSIUM BROMIDE, SODIUM BROMIDE, ZINC SULFATE ANHYDROUS, AND SULFUR	PLYMOUTH HEALTHCARE PRODUCTS LLC	f7f1c99e-1a67-4b34-b1f4-0ac38b9d8006	2025-01-07	Warnings, Adverse reactions	Exact identifier ndc (package): 61480-137-05 ndc (product): 61480-137 ndc11 (package): 61480013705

Reported adverse events (FAERS/openFDA)#

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