NDC11 75053000301

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
75053-0003-0175053-0003
75053-0003-175053-0003
75053-003-0175053-003

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
CelltemCARBO VEGETABILIS, ANILINUM, RADIUM BROMATUM, MILLEFOLIUM, MEDULLA OSSIS SUIS, RNA, DNA, METHYLENE BLUE, ABROTANUM, CALCAREA OXALICA, CONIUM MACULATUM, EUPHORBIA COROLLATA, EUPHORBIUM OFFICINARUMNucleic Products, LLCcd6670f1-d910-4228-ad8c-0bbe173e3a8c2025-03-20WarningsExact identifier
ndc (package): 75053-0003-1
ndc (product): 75053-0003
ndc11 (package): 75053000301

Reported adverse events (FAERS/openFDA)#

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