FDA.reportPublic FDA data

NDC11 00185012201

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
00185-0122-0100185-0122
00185-0122-100185-0122
00185-122-0100185-122
0185-0122-010185-0122

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
Nitrofurantoin (monohydrate/macrocrystals)NITROFURANTOIN (MONOHYDRATE/MACROCRYSTALS)Sandoz Inc7ba9a729-a73a-4a13-a336-0284cc8a67e12024-02-28Warnings, Adverse reactionsExact identifier
ndc (package): 0185-0122-01
ndc (product): 0185-0122
ndc11 (package): 00185012201

Reported adverse events (FAERS/openFDA)#

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