NDC11 51662161101

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
51662-1611-0151662-1611
51662-1611-151662-1611

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
GRAFCO SILVER NITRATE (75% SILVER NITRATE, 25% POTASSIUM NITRATE)GRAFCO SILVER NITRATE (75% SILVER NITRATE, 25% POTASSIUM NITRATE)HF Acquisition Co LLC, DBA HealthFirste5ebf7aa-fbe5-45b1-e053-2a95a90a5cbf2024-03-25WarningsExact identifier
ndc (package): 51662-1611-1
ndc (product): 51662-1611
ndc11 (package): 51662161101

Reported adverse events (FAERS/openFDA)#

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