NDC11 50090617200

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
50090-6172-0	50090-6172
50090-6172-00	50090-6172

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
SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF	POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE	A-S Medication Solutions	01131ba6-6d5b-4710-bec3-ba1769c08c79	2024-10-22	Warnings	Exact identifier ndc (package): 50090-6172-0 ndc (product): 50090-6172 ndc11 (package): 50090617200

Reported adverse events (FAERS/openFDA)#

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