FDA.reportPublic FDA data

NDC11 69339013602

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
69339-0136-0269339-0136
69339-0136-269339-0136
69339-136-0269339-136

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 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DiazepamDIAZEPAMNatco Pharma USA LLC6b8dc373-fa01-42c9-89af-4e00bf00180a2026-02-12Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 69339-136-02
ndc (product): 69339-136
ndc11 (package): 69339013602
DiazepamDIAZEPAMNatco Pharma USA LLCa14f5930-a3ac-4996-9778-df5baa3d0bab2025-04-24Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (product): 69339-136

Reported adverse events (FAERS/openFDA)#

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