FDA.reportPublic FDA data

NDC11 00178061501

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
00178-0615-0100178-0615
00178-0615-100178-0615
00178-615-0100178-615
0178-0615-010178-0615

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
UROCIT-KPOTASSIUM CITRATEMission Pharmacal Company72cdea1b-2240-41db-987d-86d5c6aaa9782021-12-02Warnings, Adverse reactionsExact identifier
ndc (package): 0178-0615-01
ndc (product): 0178-0615
ndc11 (package): 00178061501

Reported adverse events (FAERS/openFDA)#

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