NDC 85766-067

This exact product or package identity exists in FDA auxiliary data but is not present in the current primary NDC product table. The package identity is preserved; status rows are reported source observations, not medical conclusions.

Requested NDC
85766-067
Product root
85766-067
Identity scope
Product
Primary current NDC product row
Not present

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 9 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct85766-067DDiscontinued by firm2026-10-05
excluded packagepackage85766-06785766-067-01DDiscontinued by firm2026-10-05
excluded packagepackage85766-06785766-067-05DDiscontinued by firm2026-10-05
excluded packagepackage85766-06785766-067-15DDiscontinued by firm2026-10-05
excluded packagepackage85766-06785766-067-20DDiscontinued by firm2026-10-05
excluded packagepackage85766-06785766-067-21DDiscontinued by firm2026-10-05
excluded packagepackage85766-06785766-067-30DDiscontinued by firm2026-10-05
excluded packagepackage85766-06785766-067-60DDiscontinued by firm2026-10-05
excluded packagepackage85766-06785766-067-90DDiscontinued by firm2026-10-05

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BenzonatateBENZONATATESportpharm LLCdf48d617-a3c2-4776-937d-ccfca651d4fc2026-07-23Warnings, Adverse reactionsExact identifier
ndc (product): 85766-067

Reported adverse events (FAERS/openFDA)#

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