NDC11 50742039305

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
50742-0393-05	50742-0393
50742-0393-5	50742-0393
50742-393-05	50742-393

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	Ingenus Pharmaceuticals, LLC	e14f5fd6-d01a-489d-9baa-61778b1352a8	2024-10-22	Warnings, Adverse reactions	Exact identifier ndc (package): 50742-393-05 ndc (product): 50742-393 ndc11 (package): 50742039305

Reported adverse events (FAERS/openFDA)#

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