NDC11 55150015520

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
55150-0155-20	55150-0155
55150-155-20	55150-155

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
Acyclovir Sodium	ACYCLOVIR SODIUM	Eugia US LLC	ae921e4e-b8ae-4a45-acc1-32e5e719812b	2023-07-05	Warnings, Adverse reactions	Exact identifier ndc (package): 55150-155-20 ndc (product): 55150-155 ndc11 (package): 55150015520
Acyclovir Sodium	ACYCLOVIR SODIUM	AuroMedics Pharma LLC	d3ab226c-677d-4cb7-85cb-1c2e5012f40d	2017-09-18	Warnings, Adverse reactions	Exact identifier ndc (product): 55150-155

Reported adverse events (FAERS/openFDA)#

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