NDC11 59651018330

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
59651-0183-30	59651-0183
59651-183-30	59651-183

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
ALBUTEROL SULFATE	ALBUTEROL SULFATE	Aurobindo Pharma Limited	78e6bee2-7113-46cf-8c97-dc61b0f7b94f	2024-07-31	Warnings, Adverse reactions	Exact identifier ndc (package): 59651-183-30 ndc (product): 59651-183 ndc11 (package): 59651018330

Reported adverse events (FAERS/openFDA)#

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