NDC11 55150011899

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
55150-0118-99	55150-0118
55150-118-99	55150-118

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ampicillin and Sulbactam	AMPICILLIN SODIUM AND SULBACTAM SODIUM	Eugia US LLC	437a26f4-776b-4f74-99b2-09ad79831b0c	2025-12-18	Warnings, Adverse reactions	Exact identifier ndc (product): 55150-118
Ampicillin and Sulbactam	AMPICILLIN SODIUM AND SULBACTAM SODIUM	Eugia US LLC	2709e9fc-2341-4382-af72-c2e3201bd77a	2025-08-12	Warnings, Adverse reactions	Exact identifier ndc (package): 55150-118-99 ndc (product): 55150-118 ndc11 (package): 55150011899

Reported adverse events (FAERS/openFDA)#

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