NDC11 68682010630

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
68682-0106-3068682-0106
68682-106-3068682-106

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
NifedipineNIFEDIPINEOceanside Pharmaceuticalsfb6d8f32-198e-4ccf-bf25-069c03d624fd2026-02-09Warnings, Adverse reactionsExact identifier
ndc (package): 68682-106-30
ndc (product): 68682-106
ndc11 (package): 68682010630

Reported adverse events (FAERS/openFDA)#

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