FDA.reportPublic FDA data

NDC11 00019132365

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 NDCProduct root
00019-1323-6500019-1323
0019-1323-650019-1323

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 ยท 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Optiray 320IOVERSOLLiebel-Flarsheim Company LLC6cb6ca5f-b249-49b0-a9eb-8aa583da7c742025-12-29Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (product): 0019-1323
Optiray 320IOVERSOLLiebel-Flarsheim Company LLCcd718d1c-f813-4114-a50d-c744ff7eb1bf2025-12-29Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 0019-1323-65
ndc (product): 0019-1323
ndc11 (package): 00019132365
Optiray 320IOVERSOLLiebel-Flarsheim Company LLC549d38db-d4ed-4708-8f76-7cdaa157063f2023-02-17Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (product): 0019-1323

Reported adverse events (FAERS/openFDA)#

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