FDA.reportPublic FDA data

NDC11 00591268201

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
00591-2682-0100591-2682
00591-2682-100591-2682
0591-2682-010591-2682

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 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Potassium CitratePOTASSIUM CITRATEActavis Pharma, Inc.ac173781-486b-461c-97ae-8b5c69e207922022-06-01Warnings, Adverse reactionsExact identifier
ndc (package): 0591-2682-01
ndc (product): 0591-2682
ndc11 (package): 00591268201

Reported adverse events (FAERS/openFDA)#

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