NDC 83663-002-01 - REUS NR

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
83663-002
Requested NDC
83663-002-01
Package NDCs from labels
83663-002-01, 83663-002-02
Manufacturer
REUS POLSKA SP Z O O
Effective date
2023-08-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
REUS NR - REUS POLSKA SP Z O OREUS POLSKA SP Z O O2023-08-29HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83663-002-022024-07-30C16284748780-11030e365-24cb-111a-e063-dadaa90a10e2040bfcf7-f511-2fa1-e063-6394a90a5ef9
83663-002-022024-01-30C16284748780-11030e365-24cb-111a-e063-dadaa90a10e2040bfcf7-f511-2fa1-e063-6394a90a5ef9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83663-002-01REUS NR80 in 1 BOTTLECAPSULE801
83663-002-02REUS NR80 in 1 BOTTLECAPSULE801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83663-002REUS NR CAPSULE [REUS POLSKA SP Z O O]12 package rows20230915_040bfcf7-f511-2fa1-e063-6394a90a5ef9.zip

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
040bfcf7-f512-2fa1-e063-6394a90a5ef9040bfcf7-f511-2fa1-e063-6394a90a5ef92023-08-29Boxed warning, WarningsExact identifier
spl id: 040bfcf7-f512-2fa1-e063-6394a90a5ef9
spl set id: 040bfcf7-f511-2fa1-e063-6394a90a5ef9

Reported adverse events (FAERS/openFDA)#

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