NDC11 55150033501

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
55150-0335-01	55150-0335
55150-0335-1	55150-0335
55150-335-01	55150-335

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
CARBOPLATIN	CARBOPLATIN	Eugia US LLC	5abfcb87-bb02-4384-9c9d-7d0e3e809311	2025-01-30	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (product): 55150-335
CARBOPLATIN	CARBOPLATIN	Eugia US LLC	f5fe9a20-47a5-45b9-ab06-c6158d9b6aca	2025-01-10	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 55150-335-01 ndc (product): 55150-335 ndc11 (package): 55150033501

Reported adverse events (FAERS/openFDA)#

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